WO1999032467A1

WO1999032467A1 - 1,2,4-benzothiadiazine derivatives, their preparation and use

Info

Publication number: WO1999032467A1
Application number: PCT/DK1998/000546
Authority: WO
Inventors: Pascal De Tullio; Flemming Elmelund Nielsen; John Bondo Hansen; Holger Claus Hansen; Bernard Pirotte; Stéphane Boverie; Fabian Somers; Philippe Lebrun; John Patrick Mogensen
Original assignee: Novo Nordisk A/S
Priority date: 1997-12-19
Filing date: 1998-12-11
Publication date: 1999-07-01
Also published as: AU1555999A; ZA9811651B

Abstract

1,2,4-benzothiadiazine derivatives of general formula (I) wherein R?3, R5, R6, R7, R8¿ and Z are defined in the description, compositions thereof and methods for preparing the compounds are described. The compounds are useful in the treatment of diseases of the central nervous system, the cardiovascular system, the pulmonary system, the gastrointestinal system and the endocrinological system.

Description

1.2.4-Benzothiadiazine Derivatives, their Preparation and Use

FIFI-.n OF THE INVENTION

The present invention relates to 1 ,2,4-benzothiadiazine derivatives, to methods for their preparation, to compositions comprising the compounds, to the use of these compounds as medicaments and their use in therapy e.g. in the treatment of diseases of the central nervous system, the cardiovascular system, the pulmonary system, the gastrointestinal system and the endocrinological system.

BACKGROUND OF THE INVENTION

Potassium channels play an important role in the physiological and pharmacological control of cellular membrane potential. Amongst the different types of potassium channels are the ATP-sensitive (K_ATP-) channels which are regulated by changes in the intracellular concentration of adenosine triphosphate. The K_ATP-channels have been found in cells from various tissues such as cardiac cells, pancreatic cells, skeletal muscles, smooth muscles, central neurons and adenohypophysis cells. The channels have been associated with diverse cellular functions for example hormone secretion (insulin from pancreatic beta- cells, growth hormone and prolactin from adenohypophysis cells), vasodilation (in smooth muscle cells), cardiac action potential duration, neurotransmitter release in the central nervous system.

Modulators of the K_ATP-channels have been found to be of importance for the treatment of various diseases. Certain sulphonylureas which have been used for the treatment of non- insulin-dependent diabetes mellitus act by stimulating insulin release through an inhibition of the K_ATP -channels on pancreatic beta-cells.

The potassium channel openers, which comprise a heterogeneous group of compounds, have been found to be able to relax vascular smooth muscles and have therefore been used for the treatment of hypertension.

In addition, potassium channel openers can be used as bronchodilators in the treatment of asthma and various other diseases. Furthermore, potassium channel openers have been shown to promote hairgrowth, and have been used for the treatment of baldness.

Potassium channel openers are also able to relax urinary bladder smooth muscle and therefore, can be used for the treatment of urinary incontinence. Potassium channel openers which relax smooth muscle of the uterus can be used for treatment of premature labour.

By acting on potassium channels of the central nervous system these compounds can be used for treatment of various neurological and psychiatric diseases such as Alzheimer, epilepsy and cerebral ischemia.

Further, the compounds are found to be useful in the treatment of benign prostatic hyperplasia, erectile dysfunction and in contraception.

Compounds of the present invention, which inhibit insulin secretion by activating potassium channels of the beta-cell can be used in combination with other compounds which may be used to treat non-insulin dependent diabetes mellitus and insulin dependent diabetes mellitus. Examples of such compounds are insulin, insulin sensitizers, such as thiazolidinediones, insulin secretagogues, such as repaglinide, tolbutamide, glibenclamide and glucagon like peptide ( GLP1), inhibitors of α-glucosidases and hepatic enzymes responsible for the biosynthesis of glucose.

Recently, it has been shown that Diazoxide (7-chloro-3-methyl-2H-1 ,2,4-benzothiadiazine 1 ,1 -dioxide) and certain 3-(alkylamino)-4H-pyrido[4,3-e]-1 ,2,4-thiadiazine 1 ,1 -dioxide derivatives inhibit insulin release by an activation of K_ATP-channels on pancreatic beta-cells (Pirotte B. et al. Biochem. Pharmacol, 4Z, 1381-1386 (1994); Pirotte B. et al., J. Med. Chem., 3f>, 3211-3213 (1993). Diazoxide has furthermore been shown to delay the onset of diabetes in BB-rats ( Vlahos WD et al. Metabolism 40, 39-46 (1991)). In obese zucker rats diazoxide has been shown to decrease insulin secretion and increase insulin receptor binding and consequently improve glucose tolerance and decrease weight gain (Alemzadeh R. et al. Endocrinol. 133. 705-712, 1993). It is expected that compounds which activate K_ATP-channels can be used for treatment of diseases characterised -by an overproduction of insulin and for the treatment and prevention of diabetes. EP 618 209 discloses a class of pyridothiadiazine derivatives having an alkyl or an alkylamino group in position 3 of the thiadiazine ring. These compounds are claimed to be agonists at the A PA-glutamate receptor.

In J. Med. Chem. 1980, 23, 575-577 the synthesis of 4(5)-amino-and formylaminoimidazo- 5(4) carboxamide and their properties as agents of chemotherapeutic value are described. Especially, the compounds 3-aminoimidazo[4,5-e]-1 ,2,4-thiadiazine 1 ,1 -dioxide and N- benzoylaminoimidazo[4,5-e]-1 ,2,4-thiadiazine 1 ,1 -dioxide are shown.

DESCRIPTION OF THE INVENTION

The present invention relates to 1 ,2,4-benzothiadiazine derivatives of the general formula

wherein

Z is O, S, S(=O), S(=O)₂, S(=NR), S(=O)(=NR) or S(=NR)₂

wherein R is hydrogen; C,.₆-alkyl, C_2-6-alkeπyl or C_2-6-alkynyl optionally mono- or polysub- stituted with halogen, hydroxy or C_1-6-alkoxy; or C^-cycloalkyl optionally mono- or polysubstituted with C^-alkyl, halogen, hydroxy or C^-alkoxy;

R³ is C^-cycloalkyl or (C₃.₆-cycloalkyl)C_1-6-alkyl the C^-cycloalkyl group optionally being mono- or polysubstituted with C^-alky!, halogen, hydroxy or C_1-6-alkoxy; a 3-6 membered saturated ring system comprising one or more nitrogen-, oxygen- or sulfur atoms, optionally being mono- or polysubstituted with halogen, cyano, trifluoromethyl, C,.₆-alkyl, C_1-6-alkoxy, C₁.₆-alkoxy-C₁_₆-alkyl, aryl, arylalkyl, hydroxy, oxo, nitro, amino, C_1-6-monoalkyl or dialkylamino; or straight or branched C_1-18-alkyl, C₂.₁₈-alkenyl or C₂.₁₈-alkynyl, each of the groups being optionally mono- or polysubstituted with halogen, hydroxy, C_1-6-alkoxy, C_1-6- alkylthio, C₃.₆-cycloalkyl, nitro, amino, C_1-6- monoalkyl- or dialkylamino, cyano, ^"oxo, formyl, acyl, carboxy, C_1-6-alkoxycarbonyl, carbamoyl, formylamino, or C,_₆-alkylcarbonylamino, aryl, aryioxy, arylalkoxy, the aryl group optionally being mono- or polysubstituted with C,^- alkyl, perhalomethyl, halogen, hydroxy or C^-alkoxy; bicycloalkyl, aryl, heteroaryl, arylalkyl or heteroarylalkyl, each of the groups being optionally mono- or polysubstituted with halogen, hydroxy, C_1-6-alkyl, C_1-6-alkoxy, aryioxy, arylalkoxy, nitro, amino, C_1-6- monoalkyl- or dialkylamino, cyano, oxo, acyl or C_1-6-alkoxycarbonyl;

or R³ is

wherein n, m and p independently are 0, 1 , 2 or 3 and R¹⁰ is hydrogen; hydroxy; C_1-6- alkoxy; C^s-cycloalkyl optionally mono- or polysubstituted with C,.₆-alkyl, halogen, hydroxy or C_1-6-alkoxy; C^-alkyl, C₂.₆-alkenyl or C₂.₆-alkynyl optionally mono- or polysubstituted with halogen;

R⁵, R⁶, R⁷, R⁸ independently are hydrogen, halogen; C_1-18-alkyl; C^-cycloalkyl; hydroxy; C-,. ₆-alkoxy;

nitro; amino; cyano; cyanomethyl; perhalomethyl; C,-₆- monoalkyl- or dialkylamino; sulfamoyl; C^-alkylthio; C^-alkylsulfonyl; C_1-6-alkylsulfinyl; C,. ₆-alkylcarbonylamino; arylthio, arylsulfinyl, arylsulfonyl, aryl, arylalkyl, aryioxy, the aryl group optionally being mono- or polysubstituted with C_1-6-alkyl, perhalomethyl, halogen, hydroxy or C_1-6-alkoxy; C^-alkoxycarbonyl; C₁.₆-alkoxycarbonyl-C₁.₆-alkyl; carbamyl; carbamylmethyl; C^-monoalkyl- or dialkylaminocarbonyl; C^-monoalkyl- or dialkylami- nothiocarbonyl; ureido; C_Lg-monoalkyl- or dialkylaminocarbonylamino, thiocarbamyl; thioureido; C^-monoalkyl- or dialkylaminothiocarbonylamino; Cj.s-monoalkyl- or dialky- laminosulfonyl; carboxy; carboxy-C_1-6-alkyl; acyl; formyl; or a 5 - 6 membered nitrogen, oxygen or sulfur containing ring, optionally substituted with C^-alkyl or phenyl, the phenyl group optionally being mono- or polysubstituted with C,.₆-alkyl, perhalomethyl, halogen, hydroxy or C_1-6-alkoxy;

or a salt thereof with a pharmaceutically acceptable acid or base.

Within its scope the invention includes all optical isomers of compounds of formula I, some of which are optically active, and also their mixtures including racemic mixture thereof.

The scope of the invention also includes all tautomeric forms of the compounds of formula I.

The salts include pharmaceutically acceptable acid addition salts, pharmaceutically acceptable metal salts or optionally alkylated ammonium salts, such as hydrochloric, hydrobromic, hydroiodic, phosphoric, sulfuric, trifluoroacetic, trichloroacetic, oxalic, maleic, pyruvic, malonic, succinic, citric, tartaric, fumaric, mandelic, benzoic, cinnamic, methane- sulfonic, ethane sulfonic, picric and the like, and include acids related to the pharmaceutically acceptable salts listed in Journal of Pharmaceutical Science, 66_, 2 (1977) and incorporated herein by reference, or lithium, sodium, potassium, magnesium and the like.

The term "C_1-6-alkoxy" as used herein, alone or in combination, refers to a straight or branched monovalent substituent comprising a C^-alky! group linked through an ether oxygen having its free valence bond from the ether oxygen and having 1 to 6 carbon atoms e.g. methoxy, ethoxy, propoxy, isopropoxy, butoxy, pentoxy.

The term "C^-alkylthio" as used herein, alone or in combination, refers to a straight or branched monovalent substituent comprising a lower alkyl group linked through a divalent sulfur atom having its free valence bond from the sulfur atom and having 1 to 6 carbon atoms e.g. methylthio, ethylthio, propylthio, butylthio, pentylthio.

The terms "C₂.₆-alkenyl" and "C₂.₁₈-alkenyl" as used herein refers to an unsaturated hydrocarbon chain having 2-6 or 2-18 carbon atoms and one double bond such as e.g. vinyl, 1-propenyl, allyl, isopropenyl, n-butenyl, n-pentenyl and n-hexenyl. The term "C₃.₆-cycloalkyr as used herein refers to a radical of a saturated cyclic hydrocarbon with the indicated number of carbons such as cyclopropyi, cyclobutyl, cyclopentyl, or cyclohexyl.

The terms "C₂.₆-alkynyl" and "C₂.₁₈-alkynyl" as used herein refers to unsaturated hydrocarbons which contain triple bonds, such as e.g. -C≡CH, -CsCCH₃, -CH₂C≡CH, -CH₂CH₂C≡CH, -CH(CH₃)C=CH, and the like.

The term "C^-alkoxy-C^-alkyl" as used herein refers to a group of 2-12 carbon atoms interrupted by an O such as e.g. CH₂-O-CH₃, CH₂-O-CH₂-CH₃, CH₂-O-CH(CH₃)₂ and the like.

The term "halogen" means fluorine, chlorine.-bromine or iodine.

The term "perhalomethyl" means trifluoromethyl, trichloromethyl, tribromomethyl or triiodomethyl.

The terms "C_1-6-alkyl", "C_1-12-alkyl" and "C_1-18-alkyr as used herein, alone or in combination, refers to a straight or branched, saturated hydrocarbon chain having the indicated number of carbon atoms such as e.g. methyl, ethyl, n-propyl, isopropyl, n-butyl, sec-butyl, isobutyl, tert-butyl, n-pentyl, 2-methylbutyl, 3-methylbutyl, 4-methylpentyl, neopentyl, n-hexyl, 1 ,2- dimethylpropyl, 2,2-dimethylpropyl, 1 ,2,2-trimethylpropyl and the like. The term ^uC_1-18-alkyr as used herein also includes secondary C^-alkyl and tertiary C_4-6-alkyl.

The term "C_1-6-monoalkylamino" as used herein refers to an amino group wherein one of the hydrogen atoms is substituted with a straight or branched, saturated hydrocarbon chain having the indicated number of carbon atoms such as e.g. methylamino, ethylamino, propylamino, n-butylamino, sec-butylamino, isobutylamino, tert-butylamino, n-pentylamino, 2-methylbutylamino, n-hexylamino, 4-methylpentylamino, neopentylamino, n-hexylamino, 2,2-dimethylpropylamino and the like.

The term "C^-dialkylamino" as used herein refers to an amino group wherein the two hydrogen atoms independently are substituted with a straight or branched, saturated hydrocarbon chain having the indicated number of carbon atoms; such as dimethylamino, N-ethyl-N-methylamino, diethylamino, dipropylamino, N-(n-butyl)-N-methylamino, di(n- pentyl)amino, and the like.

The term "acyl" as used herein refers to a monovalent substituent comprising a C_1-6-alkyl group linked through a carbonyl group; such as e.g. acetyl, propionyl, butyryl, isobutyryl, pivaloyl, valeryl, and the like.

The term "C_Le-alkoxycarbonyl" as used herein refers to a monovalent substituent comprising a C^-alkoxy group linked through a carbonyl group; such as e.g. methoxycar- bonyl, carbethoxy, propoxycarbonyl, isopropoxycarbonyl, n-butoxycarbonyl, sec- butoxycarbonyl, tert-butoxycarbonyl, 3-methylbutoxycarbonyl, n-hexoxycarbonyl and the like.

The term "3-6 membered saturated ring system" as used herein refers to a monovalent substituent comprising a monocyclic saturated system containing one or more hetero atoms selected from nitrogen, oxygen and sulfur and having 3-6 members and having its free valence from a carbon atom, e.g. 2-pyrrolidyl, 4-piperidyl, 3-morpholinyl, 1 ,4-dioxan-2- yl, 5-oxazolidinyl, 4-isoxazolidinyl, or 2-thiomorpholinyl.

The term "bicycloalkyl" as used herein refers to a monovalent substituent comprising a bicyclic structure made of 6-12 carbon atoms such as e.g. 2-norbornyl, 7-norbornyl, 2- bicyclo[2.2.2]octyl, and 9-bicyclo[3.3.1]nonanyl.

The term "aryl" as used herein refers to phenyl, 1-naphthyl, or 2-naphthyl.

The term "heteroaryl" as used herein, alone or in combination, refers to a monovalent substituent comprising a 5-6 membered monocyclic aromatic system or a 9-10 membered bicyclic aromatic system containing one or more heteroatoms selected from nitrogen, oxygen and sulfur, e.g. pyrrole, imidazole, pyrazole, triazole, pyridine, pyrazine, pyrimidine, pyridazine, isothiazole, isoxazole, oxazole, oxadiazole, thiadiazole, quinoline, isoquinoline, quinazoline, quinoxaline, indole, benzimidazole, benzofuran, pteridine, and purine. The term "arylalkyl" as used herein refers to a straight or branched saturated carbon chain containing from 1 to 6 carbons substituted with an aromatic carbohydride; such as benzyl, phenethyl, 3-phenylpropyl, 1-naphtyimethyl, 2-(1-naphtyl)ethyl and the like.

The term "aryioxy" as used herein refers to phenoxy, 1-naphthyloxy or 2-naphthyloxy.

The term "arylalkoxy" as used herein refers to a C^-alkoxy group substituted with an aromatic carbohydride, such as benzyloxy, phenethoxy, 3-phenylpropoxy, 1- naphthylmethoxy, 2-(1-naphtyl)ethoxy and the like.

The term "C...₆-alkylsulfonyr as used herein refers to a monovalent substituent comprising a Ci-e-alkyl group linked through a sulfonyl group such as e.g. methylsulfonyl, ethylsul- fonyl, n-propylsulfonyl, isopropylsulfonyl, n-butylsulfonyl, sec-butylsulfonyl, iso- butylsulfonyl, tert-butylsulfonyl, n-pentylsulfonyl, 2-methylbutylsulfonyl, 3- methylbutylsulfonyl, n-hexylsulfonyl, 4-methylpentylsulfonyl, neopentylsulfonyl, n- hexylsulfonyl and 2,2-dimethylpropylsulfonyl.

The term "C_Ls-monoalkylaminosulfonyl" as used herein refers to a monovalent substituent comprising a C_Lβ-monoalkylamino group linked through a sulfonyl group such as e.g. methylaminosulfonyl, ethylaminosulfonyl, n-propylaminosulfonyl, isopropylaminosulfonyl, n-butylaminosulfonyl, sec-butylaminosulfonyl, isobutylaminosulfonyl, tert- butylaminosulfonyl, n-pentylaminosulfonyl, 2-methylbutylaminosulfonyl, 3- methylbutylaminosulfonyl, n-hexylaminosulfonyl, 4-methylpentylaminosulfonyl, neopenty- laminosulfonyl, n-hexylaminosulfonyl and 2,2-dimethylpropylaminosulfonyl.

The term "C..₆-dialkylaminosulfonyr as used herein refers to a monovalent substituent comprising a C_1-6-dialkylamino group linked through a sulfonyl group such as dimethylami- nosulfonyl, N-ethyl-N-methylaminosulfonyl, diethylaminosulfonyl, dipropylaminosulfonyl, N- (n-butyl)-N-methylaminosulfonyl, di(n-pentyl)aminosulfonyl, and the like.

The term "C_1-6-alkylsulfinyl" as used herein refers to a monovalent substituent comprising a straight or branched C_1-6-alkyl group linked through a sulfinyl group (-S(=O)-); such as e.g. methylsulfinyl, ethylsulfinyl, isopropylsulfinyl, butylsulfinyl, pentylsulfinyl, and the like. The term "C_1-6-alkylcarbonylamino" as used herein refers to an amino group wherein one of the hydrogen atoms is substituted with an acyl group, such as e.g.^' acetamido, propiona- mido, isopropylcarbonylamino, and the like.

The term "(C-^-cycloalky C^-alkyl" as used herein, alone or in combination, refers to a straight or branched, saturated hydrocarbon chain having 1 to 6 carbon atoms and being monosubstituted with a C^-cycloalkyl group, the cycloalkyl group optionally being mono- or polysubstituted with C_1-6-alkyl, halogen, hydroxy or C^-alkoxy; such as e.g. cyclopropylme- thyl, (l-methylcyclopropyl)methyl, 1-(cyclopropyl)ethyl, cyclopentylmethyl, cyclohexylmethyl, and the like.

The term "arylthio" as used herein, alone or in combination, refers to an aryl group linked through a divalent sulfur atom having its free valence bond from the sulfur atom, the aryl group optionally being mono- or polysubstituted with C_1-6-alkyl, halogen, hydroxy or C^- alkoxy; e.g. phenylthio, (4-methylphenyl)- thio, (2-chlorophenyl)thio, and the like.

The term "arylsulfinyl" as used herein refers to an aryl group linked through a sulfinyl group (- S(=0)-), the aryl group optionally being mono- or polysubstituted with C_1-6-alkyl, halogen, hydroxy or C^-alkoxy; such as e.g. phenylsulfinyl, (4-chlorophenyl)sulfinyl, and the like.

The term "arylsulfonyl" as used herein refers to an aryl group linked through a sulfonyl group, the aryl group optionally being mono- or polysubstituted with C^-alkyl, halogen, hydroxy or C_1-6-alkoxy; such as e.g. phenylsulfonyl, tosyl, and the like.

The term "C^-monoalkylaminocarbonyl" as used herein refers to a monovalent substituent comprising a C^-monoalkylamino group linked through a carbonyl group such as e.g. methylaminocarbonyl, ethylaminocarbonyi, n-propylaminocarbonyl, isopropylaminocarbonyl, n-butylaminocarbonyl, sec-butylaminocarbonyl, isobutylaminocarbonyl, tert- butylaminocarbonyl, n-pentylaminocarbonyl, 2-methylbutylaminocarbonyl, 3- methylbutylamino-carbonyl, n-hexylaminocarbonyl, 4-methylpentylaminocarbonyl, neo- pentylaminocarbonyl, n-hexylaminocarbonyl and 2-2-dimethylpropylaminocarbonyl. The term "d-g-dialkylaminocarbonyl" as used herein refers to a monovalent substituent comprising a C_1-6-dialkylamino group linked through a carbonyl group such as dimethylami- nocarbonyl, N-ethyl-N-methylaminocarbonyl, diethylaminocarbonyl, dipropylaminocarbonyl, N-(n-butyl)-N-methylaminocarbonyl, di(n-pentyl)aminocarbonyl, and the like. 5 The term "C^-monoalkylaminocarbonylamino" as used herein refers to an amino group wherein one of the hydrogen atoms is substituted with a C_1-6-monoalkylaminocarbonyl group, e.g. methylaminocarbonylamino, ethylaminocarbonylamino, n-propylaminocarbonylamino, isopropylaminocarbonylamino, n-butylaminocarbonylamino, sec-butyiaminocarbonylamino, o isobutyiaminocarbonylamino, tert-butylaminocarbonylamino, and 2- methylbutylaminocarbonylaminό.

The term "Ci-e-dialkylaminocarbonylamino" as used herein refers to an aminσgroup wherein one of the hydrogen atoms is substituted with a C^-dialkylaminocarbonyl group, such as 5 dimethylaminocarbonylamino, N-ethyl-N-methylaminocarbonylamino, diethyla- minocarbonylamino, dipropylaminocarbonylamino, N-(n-butyl)-N- methylaminocarbonylamino, di(n-pentyl)aminocarbonylamino, and the like.

The term "5- or 6-membered nitrogen, oxygen or sulfur containing ring" as used herein 0 refers to a monovalent substituent comprising a monocyclic unsaturated or saturated system containing one or more nitrogen, oxygen or sulfur atoms and having 5 or 6 members, e.g. pyrrolidinyl, pyrrolinyl, imidazolidinyl, pyrazolidinyl, pyrazolinyl, piperidyl, piperazinyl, pyrrolyl, 2H-pyrrolyl, imidazolyl, pyrazolyl, triazolyl, pyridyl, pyrazinyl, pyrimidi- nyl, pyridazinyl, morpholino, thiomorpholino, isothiazolyl, isoxazolyl, oxazolyl, oxadiazolyl, 5 thiadiazolyl, 1,3-dioxolanyl, and 1 ,4-dioxolanyl.

Preferred compounds of the invention are:

7-chloro-3-isobutylsulfanyl-4H-1 ,2,4-benzothiadiazine 1 ,1 -dioxide 0 7-chloro-3-cyclobutylsulfanyl-4H-1 ,2,4-benzothiadiazine 1 ,1 -dioxide 7-chloro-3-cyclopentylsulfanyl-4H-1 ,2,4-benzothiadiazine 1 ,1 -dioxide 7-chloro-3-(1-phenylethyl)sulfanyl-4H-1 ,2,4-benzothiadiazine 1 ,1 -dioxide 7-bromo-3-isopropylsulfanyl-4H-1 ,2,4-benzothiadiazine 1 , 1 -dioxide 7-fluoro-3-isopropylsulfanyl-4H-1 ,2,4-benzothiadiazine 1 , 1 -dioxide 6-fluoro-3-isopropylsulfanyl~4H-1 ,2,4-benzothiadiazine 1 ,1 -dioxide 6,8-dichloro-3-isopropylsulfanyl-4H-1 ,2,4-benzothiadiazine 1,1 -dioxide 6,7-dichloro-3-isopropylsulfanyl-4H-1 ,2,4-benzothiadiazine 1 ,1 -dioxide 5 6-methoxy-3-isopropylsulfanyl-4H-1 ,2,4-benzothiadiazine 1 , 1 -dioxide 7-methoxy-3-isopropylsulfanyl-4H-1 ,2,4-benzothiadiazine 1 ,1 -dioxide 7-trifluoromethyl-3-isopropylsulfanyl-4H-1 ,2,4-benzothiadiazine 1 , 1 -dioxide 6-trifluoromethyl-3-isopropylsulfanyl-4H-1 ,2,4-benzothiadiazine 1 ,1 -dioxide 7-chloro-3-ethylsulfinyl-4H-1 ,2,4-benzothiadiazine 1 , 1 -dioxide o 7-chloro-3-propylsulfinyl-4H-1 ,2,4-benzothiadiazine 1 , 1 -dioxide 7-chloro-3-isopropylsulfinyl-4H-1 ,2,4-benzotιiadiazine 1 , 1 -dioxide 7-chloro-3-ethylsulfinimidoyl-4H-1 ,2,4-benzothiadiazine 1 , 1 -dioxide 6-fluoro-3-ethylsulfinimidoyl-4l-H ,2,4-benzothiadiazine 1 , 1 -dioxide 7-chloro-3-ethylsulfonimidoyl-4H-1 ,2,4-benzothiadiazine 1 , 1 -dioxide 5 7-bromo-3-isopropoxy-4H-1 ,2,4-benzothiadiazine 1 ,1-dioxide 7-fluoro-3-isopropoxy-4H-1 ,2,4-benzothiadiazine 1 ,1 -dioxide 6-fluoro-3-isopropoxy-4H-1,2,4-benzothiadiazine 1 ,1 -dioxide 6,8-dichloro-3-isopropoxy-4H-1 ,2,4-benzothiadiazine 1 ,1-dioxide 3-isopropoxy-6-methoxy-4H-1 ,2,4-benzothiadiazine 1,1 -dioxide 0 3-isopropoxy-7-methoxy-4H-1 ,2,4-benzothiadiazine 1 ,1 -dioxide 3-isopropoxy-7-trifluoromethyl-4H-1 ,2,4-benzothiadiazine 1 ,1 -dioxide 7-chloro-3-cyclopropylmethylsulfanyl-4H-1 ,2,4-benzothiadiazine 1 ,1 -dioxide 7-chloro-3- cyclopropylmethoxy-4H-1 ,2,4-benzothiadiazine 1 ,1 -dioxide 7-Chloro-3-(3-trifluoromethylbenzylsulfanyl)-4H- ,2,4-benzothiadiazine 1 , 1 -dioxide 5 7-Chloro-3-(3-methyl-but-2-enylsulfanyl)-4H-1 ,2,4-benzothiadiazine 1 ,1 -dioxide 6-bromo-3-isopropoxy-4H-1 ,2,4-benzothiadiazine 1,1 -dioxide 6-bromo-3-isopropylsulfanyl-4H-1 ,2,4-benzothiadiazine 1,1 -dioxide 6-bromo-3-cyclopropylmethylsulfanyl-4H-1 ,2,4-benzothiadiazine 1 , 1 -dioxide 6-bromo-3-cyclopropylmethoxy-4H-1 ,2,4-benzothiadiazine 1 ,1 -dioxide 0 6-bromo-3-isobutylsulfanyl-4H-1 ,2,4-benzothiadiazine 1 ,1 -dioxide 6-bromo-3-cyclobutylsulfanyl-4H-1 ,2,4-benzothiadiazine 1 , 1 -dioxide 6-bromo-3-cyclopentylsulfanyl-4H-1 ,2,4-benzothiadiazine 1 ,1 -dioxide 6-bromo-3-(1-phenylethyl)sulfanyl-4H-1 ,2,4-benzothiadiazine 1 ,1 -dioxide 3-isopropoxy-7-methyl-4H-1 ,2,4-benzothiadiazine 1 ,1 -dioxide 3-isopropylsulfanyl-7-methyl-4H-1 ,2,4-benzothiadiazine 1 , 1 -dioxide 3-cyclopropylmethylsulfanyl-7-methyl-4H-1 ,2,4-benzothiadiazine 1 , 1 -dioxide 3-cyclopropylmethoxy-7-methyl-4H-1 ,2,4-benzothiadiazine 1 ,1 -dioxide 3-isobutylsulfanyl-7-methyl-4H-1 ,2,4-benzothiadiazine 1 ,1 -dioxide 3-cyclobutylsulfanyl-7-methyl-4H-1 ,2,4-benzothiadiazine 1 ,1 -dioxide 3-cyclopentylsulfanyl-7-methyl-4H-1 ,2,4-benzothiadiazine 1 ,1 -dioxide 3-(1 -phenylethyl)sulfanyl-7-methyl-4H-1 ,2,4-benzothiadiazine 1 , 1 -dioxide 3-cyclopropylmethoxy-7-fluoro-4H-1 ,2,4-benzothiadiazine 1 , 1 -dioxide7-chloro-3- cyclopentyloxy-4H-1 ,2,4-benzothiadiazine 1 ,1-dioxide7-fluoro-3-ethylsulfanyl-4H- 1 ,2,4-benzot iadiazine 1 , 1 -dioxide7-fluoro-3-cyclopropylmethylsulfanyl-4H-1 ,2,4- benzothiadiazine 1 , 1 -dioxide7-chloro-3-ethylsulf anyl-4H-1 ,2,4-benzothiadiazine 1 ,1 - ,dioxide7-bromo-3-ethylsulfanyl-4H-1 ,2,4-benzothiadiazine 1 , 1 -dioxide7-bromo-3- cyclopropylmethylsulfanyl-4H-1 ,2,4-benzothiadiazine 1 ,1 -dioxide3-ethylsulfanyl-6- fluoro-4H-1 ,2,4-benzothiadiazine 1 , 1 -dioxide3-cyclopropylmethylsulfanyl-6-fluoro-4H- 1 ,2,4-benzothiadiazine 1 ,1 -dioxide6-chloro-3-ethylsulfanyl-4H-1 ,2,4-benzothiadiazine 1 , 1 -dioxide6-chloro-3-isopropylsulfanyI-4H-1 ,2,4-benzothiadiazine 1 , 1 -dioxideδ-chloro- 3-cyclopropylmethylsulfanyl-4H-1 ,2,4-benzothiadiazine 1 , 1 -dioxide6-chloro-3- cyclobutylsulf anyl-4H-1 ,2,4-benzothiadiazine 1 , 1 -dioxide6-bromo-3-ethylsulf anyl-4H- 1 ,2,4-benzothiadiazine 1 ,1 -dioxide7-chloro-3-(5-chloro-2-methoxybenzyloxy)-4H-1 ,2,4- benzothiadiazine 1 , 1 -dioxide7-chloro-3-cyclobutoxy-4H-1 ,2,4-benzothiadiazine 1 ,1- dioxide7-chloro-3-(1-phenyl)ethoxy-4H-1 ,2,4-benzothiadiazine 1 ,1 -dioxide

The compounds of the present invention interact with the potassium channels and hence act as openers or blockers of the ATP-regulated potassium channels, which make them useful in the treatment of various diseases of the cardiovascular system, e.g. cerebral ischemia, hypertension, ischemic heart diseases, angina pectoris and coronary heart diseases; the pulmonary system; the gastrointestinal system; the central nervous system and the endocrinological system.

Since some K_ATP-openers are able to antagonize vasospasms in basilar or cerebral arteries the compounds of the present invention can be used for the treatment of vaso- spastic disorders such as subarachnoid haemorrhage and migraine. The compounds of the present invention may also be used for the treatment of diseases associated with decreased skeletal muscle blood flow such as Raynauds disease and intermittent claudication.

Further, the compounds of the invention may be used for the treatment of chronic airway diseases, including asthma, and for treatment of detrusor muscle instability secondary to bladder outflow obstruction and therefore for kidney stones by aiding their passage along the urethra.

The present compounds could also be used for treatment of conditions associated with disturbances in gastrointestinal mobility such as irritable bowel syndrome. Additionally these compounds can be used for the treatment of premature labour and dysmenorrhea.

Potassium channel openers hyperpolarize neurons and inhibit neurotransmitter release and it is expected that such compounds can be used for the treatment of various diseases of the central nervous system, e.g. epilepsia, ischemia and neurodegenerative diseases, and for the management of pain.

Further, potassium channel openers promote hairgrowth, therefore, the compounds of the present invention can be used for the treatment of baldness.

Potassium channel openers also relax urinary bladder smooth muscle, thus, the compounds of the present invention can be used for the treatment of urinary incontinence.

In diseases such as nesidioblastosis and insulinoma in which a hypersecretion of insulin causes severe hypoglycemia the compounds of the present invention can be used to reduce insulin secretion. In obesity hyperinsulinemia and insulin resistance is very frequently encountered. This condition could lead to the development of noninsulin dependent diabetes (NIDDM). It is expected that potassium channel openers, and hence the compounds of the present invention, can be used for reducing the hyperinsulinemia and thereby prevent diabetes and reduce obesity. In overt NIDDM treatment of hyperinsulinemia with potassium channel openers, and hence the present compounds, can be of benefit in restoring glucose sensitivity and normal insulin secretions.

In early cases of insulin dependent diabetes (IDDM) or in prediabetic cases, potassium channel openers and hence the present compounds can be used to induce pancreatic cell rest which may prevent the progression of the autoimmune disease.

The potassium channel openers of the present invention can be administered in combination with an immunosuppressant or with an agent like nicotinamide, which will reduce autoimmune degeneration of beta-cells.

Combining beta-cell rest with a treatment protecting the beta-cells against cytokine mediated beta-cell impairment/cytotoxicity is another aspect of this invention. Insulin requiring or Type 1 diabetes (IDDM) as well as late onset IDDM (also known as type 1.5. e.g. non-insulin-requiring Type 2 (NIIDM) patients with autoreactivity against beta-cell epitopes that later turns insulin requiring) have circulating autoreactive mono- cytes/lymphocytes that homes to the islets/beta-cells and releases their cytokines. Some of these cytokines (e.g. interleukin-1b (IL-1b) , tumour necrosis factor a (TNFa) and interferon g (IFNg)) are specifically toxic to the beta-cells, e.g. through the induction of nitric oxide (NO) and other free radicals. Inhibition of this cytotoxicity, e.g. by co- administring nicotinamide (NA), a derivative hereof or other cytokine protective compounds to the prediabetic/diabetic patients treated with the PCO compound is an example of this aspect. Nicotinamide belongs to the B-vitamin family and is derived from nicotinic acid by amidation of the carboxyl group. It processes none of nicotine's pharmacological properties. NA is converted into NAD+, which acts as a coenzyme for proteins involved in tissue respiration. NA has been proposed to influence several of the putative intracellular molecular events following immune attack on the beta-cells. Animal experiments and early non-blinded experiments in humans have indicated a protective role of this compound against IDDM as well as in cytokine/immune mediated beta-cell destruction. Yet another aspect of this application concerns the use of a PCO compound alone or in combination with the inhibitor of cytokine/immune mediated beta-cell impairment , in transplantation, e.g. islet transplantation into diabetes patients. The use of one or both of these treatments may reduce the risk of rejection of the transplanted islets/beta- cells/engineered beta-cells/pancreas. Compounds of the present invention which act as blockers of K_ATP -channels can be used for the treatment of NIDDM.

Preferably, the compounds of the present invention may be used for treatment or prevention of diseases of the endocrinological system such as hyperinsulinaemia and diabetes.

Accordingly, in another aspect the invention relates to a compound of the general formula I or a pharmaceutically acceptable acid addition salt thereof for use as a therapeutically acceptable substance, preferably for use as a therapeutically acceptable substance in the treatment of hyperinsulinaemia and treatment or prevention of diabetes.

Furthermore, the invention also relates to the use of the inventive compounds of formula I as medicaments useful for treating hyperinsulinaemia and treating or preventing diabetes . Optionally, the pharmaceutical composition of the invention may comprise a compound of formula I combined with one or more other pharmacologically active compounds, e.g. an antidiabetic or other pharmacologically active material, including compounds for the treatment and/or prophylaxis of insulin resistance and diseases wherein insulin resistance is the pathophysiological mechanism. Suitable antidiabetics comprise insulin as well as orally active hypoglycaemic agents such as sulphonylureas, e.g. glibenclamide and glipizide; biguanides, e.g. metformin; benzoic acid derivatives, e.g. repaglinide;and thiazolidinediones, e.g. troglitazone and ciglitazone.

In yet another aspect, the present invention relates to methods of preparing the above mentioned compounds. The methods comprises:

a) reacting a compound of formula II: O 99/32467

1 6

wherein Y is O or S and R⁵, R⁶ , R⁷ and R⁸ are as defined above with a compound of formula III

R³-X (III)

wherein R³ is as defined above and X is a leaving group such as halogen or sulfate, preferentially chloro, bromo or iodo to form a compound of the general formula I wherein Z is O or S. The reaction may be carried out in a suitable solvent and in the presence of a base.

b) reacting a compound of formula II:

wherein Y is O and R⁵, R⁶ , R⁷ and R⁸ are as defined above with a diazo compound of formula IV

R'R"CN₂ (IV)

wherein R' and R" together as two substituents on methyl form a group R'R"CH meeting the criteria defined above for R³, to form a compound of the general formula I wherein Z is O and R³ is R'R"CH. O 99/32467

1 7

c) reacting a compound of formula V:

wherein R⁵, R⁶ , R⁷ and R⁸ are as defined above and Q is a leaving group such as halogen, preferentially chloro, bromo, iodo; amino, trimethylamino, imidazol-1-yl, methylsulfanyl, methylsulfinyl or methylsulfonyl with a compound of formula VI:

R³YH (VI)

wherein R³ is as defined above and Y is O or S to form a compound of the general formula I wherein Z is O or S. The reaction may be carried out in a suitable solvent and in the presence of a base.

d) reacting a compound of formula VII:

wherein R³, R⁵, R⁶ , R⁷ and R⁸ are as defined above with an oxidizing agent to form a compound of the general formula I wherein Z is S(=0) or S(=0)₂.

e) reacting a compound of formula VII: O 99/32467

1 8

wherein R³, R⁵, R⁶ , R⁷ and R⁸ are as defined above with an aminating agent according to known procedures, see e.g. P.D. Kennenwell, J.B. Taylor, Chem.Soc.Rev. (1980) 477- 498 and P.D. Kennenwell, J.B. Taylor, Chem.Soc.Rev. (1975) 189-209, to form a compound of the general formula VIII

wherein n is 1 or 2.

f) reacting a compound of formula VII:

wherein R³, R⁵, R⁶ , R⁷ and R⁸ are as defined above with an aminating agent and subsequently an oxidizing agent, or vice versa, according to known procedures, e.g. P.D. Kennenwell, J.B. Taylor, Chem.Soc.Rev. (1980) 477-498 and P.D. Kennenwell, J.B. Taylor, Chem.Soc.Rev. (1975) 189-209, to form a compound of the general formula I wherein Z is S(=0)(=NR). O 99/32467

1 9

g) reacting a compound of formula IX

wherein R⁵, R⁶ , R⁷ and R⁸ are as defined above with CS₂ in the presence of a base to give the corresponding sulfonylimino carbodithioate which in turn is treated with an alkylating agent of formula III

R³-X (III)

wherein R³ is as defined above and X is a leaving group such as halogen or sulfate, preferentially chloro, bromo or iodo to form a compound of formula X

which by ring-closure, e.g. by treatment with phosgene in a suitable solvent, forms a compound of the general formula I.

h) reacting a compound of formula XI O 99/32467

20

wherein R³, R⁵, R⁶, R⁷ and R⁸ are as defined above and PG is a protecting group, e.g. substituted benzyl, with chlorosulfonyl isocyanate (CI-S0₂-NCO) and subsequent ring closure folllowed by removal of the protecting group to form a compound of formula I.

The starting materials are either known compounds or compounds which may be prepared in analogy with the preparation of known compounds or in analogy with known methods as described by e.g. Huang B.-S., et al., J. Med. Chem., 23, 575-7 (1980), Ofitserov V. I. et al., Khim. Geterotsikl. Soedin., 1119-22 (russ.) (1976), Topliss J. G., U.S. 3,641 ,017 (1972), Kotovskaya S. K. et al., Khim.-Farm. Zh., 13, 54-57 (russ.) (1979), Meyer R. F., J. Heterocycl. Chem., 6, 407-408 (1969), Hattori M., Yoneda M., Goto M., Bull. Chem. Soc. Jap., 46, 1890-1 (1973), Williams T.R. and Cram D.J., J. Org. Chem., 38, 20-26 (1973), T. Iwakawa, H. Tamura, Y. Hayase, Chem.Pharm.Bull. 38(4), 1075-6 (1990), F.E. Nielsen, H.C. Hansen, J.B. Hansen, T.M. Tagmose, PCT Int. Appl. WO 97 / 26265, M.E. Arranz, S. Vega, Heterocycles 45, 1767-1774 (1997).

PHARMACOLOGICAL METHODS

The ability of the compounds to interact with potassium channels can be determined by various methods. When patch-clamp techniques (Hamiil O.P., Marty A., Neher E.,

Sakmann B. and Sigworth F.J., Plϋgers Arch., 391. 85-100 (1981)) are used the ionic current through a single channel of a cell can be recorded.

The activity of the compounds as potassium channel openers can also be measured as relaxation of rat aorta rings according to the following procedure:

A section of rat thoracic aorta between the aortic arch and the diaphragm was dissected out and mounted as ring preparations as described by Taylor P.D. et al , Brit J. Pharma- col, 111, 42-48 (1994).

After a 45 min. equilibration period under a tension of 2 g, the preparations were contracted to achieve 80% of the maximum response using the required concentration of phenylephrine. When the phenylephrine response reached a plateau, potential vasodilator/ agents were added cumulatively to the bath in small volumes using half log molar increments at 2 min intervals. Relaxation was expressed at the percentage of the contracted tension. The potency of a compound was expressed as the concentration required to evoke a 50% relaxation of the tissue.

In the pancreatic b-cell the opening of the K_ATP-channels can be determined by measuring the subsequent change in the concentration of cytoplasmic free Ca²⁺ concentration according to the method of Arkhammar P. et al. , J. Biol. Chem., 262, 5448-5454 (1987).

-Rb* efflux from a β-cell line

The RIN 5F cell line was grown in RPMI 1640 with Glutamax I, supplemented with 10 % fetal calf serum (from GibcoBRL, Scotland, UK) and maintained in an atmosphere of 5 % C0₂ / 95 % air at 37°C. The cells were detached with a Trypsin-EDTA solution (from GibcoBRL, Scotland, UK), resuspended in medium, added 1 mCi/ml ⁸⁶Rb⁺ and replated into microtiter plates (96 well cluster 3596, sterile, from Costar Corporation, MA, USA) at a density of 50000 cells/well in 100 μl/well, and grown 24 hours before use in assay.

The plates were washed 4 times with Ringer buffer (150 mM NaCl, 10 mM Hepes, 3.0 mM KCI, 1.0 mM CaCI₂, 20 mM Sucrose, pH 7.1). Eighty μl Ringer buffer and 1 μl control- or test compound dissolved in DMSO was added. After incubation 1 h at room temperature with a lid, 50 μl of the supernatant was transferred to PicoPlates (Packard Instrument Company, CT, USA) and 100 μl MicroScint40 (Packard Instrument Company, CT, USA) added. The plates were counted in TopCount (Packard Instrument Company, CT, USA) for 1 min/well at the ³²P program.

The calculation of EC₅₀ and E_max was done by SlideWrite (Advanced Graphics Software, Inc., CA, USA) using a four parameter logistic curve: y = (a-d)/(1+(x/c)°)+d, where a = the activity estimated at concentration zero, b = a slope factor, c = the concentration at the middle of the curve and, d = the activity estimated at infinite concentration. EC₅₀ = c and E_max ⁼ d, when the curve is turned of at infinite concentrations.

5 The compounds according to the invention are effective over a wide dose range. In general satisfactory results are obtained with dosages from about 0.05 to about 1000 mg, preferably from about 0.1 to about 500 mg, per day. A most preferable dosage is about 1 mg to about 100 mg per day. The exact dosage will depend upon the mode of administration, form in which administered, the subject to be treated and the body weight of the o subject to be treated, and the preference and experience of the physician or veterinarian in charge.

The route of administration may be any route, which effectively transports the active compound to the appropriate or desired site of action, such as oral or parenteral e.g. 5 rectal, transdermal, subcutaneous, intravenous, intramuscular or intranasal, the oral route being preferred.

Typical compositions include a compound of formula I or a pharmaceutically acceptable acid addition salt thereof, associated with a pharmaceutically acceptable excipient which 0 may be a carrier or a diluent or be diluted by a carrier, or enclosed within a carrier which can be in form of a capsule, sachet, paper or other container. In making the compositions, conventional techniques for the preparation of pharmaceutical compositions may be used. For example, the active compound will usually be mixed with a carrier, or diluted by a carrier, or enclosed within a carrier which may be in the form of a ampoule, capsule, 5 sachet, paper, or other container. When the carrier serves as a diluent, it may be solid, semi-solid, or liquid material which acts as a vehicle, excipient, or medium for the active compound. The active compound can be adsorbed on a granular solid container for example in a sachet. Some examples of suitable carriers are water, salt solutions, alcohols, polyethylene glycols, polyhydroxyethoxylated castor oil, gelatine, lactose, amylose, 0 magnesium stearate, talc, silicic acid, fatty acid monoglycerides and diglycerides, pentaerythritol fatty acid esters, hydroxymethylcellulose and polyvinylpyrrolidone. The formulations may also include wetting agents, emulsifying and suspending agents, preserving agents, sweetening agents or flavouring agents. The formulations of the invention may be formulated so as to provide quick, sustained, or delayed release of the active ingredient after administration to the patient by employing procedures well known in the art.

The pharmaceutical preparations can be sterilized and mixed, if desired, with auxiliary agents, emulsifiers, salt for influencing osmotic pressure, buffers and/or coloring substances and the like, which do not deleteriously react with the active compounds.

For parenteral application, particularly suitable are injectable solutions or suspensions, preferably aqueous solutions with the active compound dissolved in polyhydroxylated castor oil.

Tablets, dragees, or capsules having talc and/or a carbohydrate carrier or binder or the like are particulariy suitable for oral application. Preferable carriers for tablets, dragees, or capsules include lactose, corn starch, and/or potato starch. A syrup or elixir can be used in cases where a sweetened vehicle can be employed.

Generally, the compounds are dispensed in unit form comprising from about 1 to about 100 mg in a pharmaceutically acceptable carrier per unit dosage.

A typical tablet, appropriate for use in this method, may be prepared by conventional tabletting techniques and contains:

Active compound 5.0 mg Lactosum 67.8 mg Ph.Eur.

Avicel® 31.4 mg

Amberlite® 1.0 mg

Magnesii stearas 0.25 mg Ph.Eur.

EXAMPLES

The process of preparing the compounds of formula I is further illustrated in the following examples which, however, are not to be construed as limiting. Intermediates

General procedure for the preparation of 2,3-dihydro-3-oxo-4H-1 ,2,4-benzothiadiazine 1 , 1 -dioxides

The compounds were obtained as described by Girard (Y. Girard et al., J. Chem. Soc. Perkin I, 1043, 1 979) using nitromethane as the solvent for the reaction of the appropriate aniline with chlorosulfonyl isocyanate. The crude product was purified by dissolution in a 5 % w/v aqueous solution of sodium hydrogen carbonate (20-30 mL/g) or in a 2.5 % w/v niethanol-water 1 : 1 solution of sodium hydrogen carbonate (40-60 mL/g). The resulting suspension or solution was treated with charcoal, filtered, and the filtrate was adjusted to pH 0 with 1 2N HCI. The precipitate was collected by filtration, washed with water and dried (yields: 40-60 %).

In this way compounds previously described as well as the following new compounds could be made:

7-Fluoro-2,3-dihydro-3-oxo-4H-1 ,2,4-benzothiadiazine 1 , 1 -dioxide; mp 275-277 °C

6-Fluoro-2,3-dihydro-3-oxo-4H-1 ,2,4-benzothiadiazine 1 , 1 -dioxide The crude compound which contains the 8-fluoro-substituted derivative as a contami- nent was purified by successive crystallization in hot water and methanol-ether. The compound however may contain a residual trace of the 8-fluoro-substituted derivative and is used without further purification; mp 260-262 °C

6-Bromo-2,3-dihydro-3-oxo-4H-1 ,2,4-benzothiadiazine 1 , 1 -dioxide The crude compound which contains the 8-bromo-substituted derivative as a contami- nent was purified by successive crystallization in hot water (two fold); mp > 300 °C

General procedure for the preparation of 3-thioxo-2,3-dihydro-4H-1 ,2,4- benzothiadiazine 1 , 1 -dioxides The appropriate 2,3-dihydro-3-oxo-4H-1 ,2,4-benzothiadiazine 1 , 1 -dioxide (0.1 mol) and phosporus pentasulfide (40-60 g) in anhydrous pyridine (250-300 mL) was reffuxed for 4-10 h (until completion of the reaction monitored by t.l.c). The solvent was removed by distillation under reduced pressure. The residue was dissolved in 2.5M NaOH (600 mL). The solution was treated with charcoal, filtered, and the filtrate was adjusted to pH 0 with 1 2N HCI. The precipitate was collected by filtration, washed with water and dissolved in a hot 5 % w/v aqueous solution of sodium hydrogen carbonate (400-600 mL) or in a 2.5 % w/v methanol-water 1 : 1 solution of sodium hydrogen carbonate (800 mL). The resulting suspension was treated with charcoal, filtered, and the filtrate was adjusted to pH 0. The precipitate was collected by filtration, washed with^' water and dried (yields: 60-80%).

7-Bromo-2,3-dihydro-3-thioxo-4H-1 ,2,4-benzothiadiazine 1 , 1 -dioxide; mp 209-21 1 °C

7-Fluoro-2,3-dihydro-3-thioxo-4H-1 ,2,4-benzothiadiazine 1 , 1 -dioxide; mp 1 93-1 95 °C

6-Bromo-2,3-dihydro-3-thioxo-4H-1 ,2,4-benzothiadiazine 1 , 1 -dioxide; mp 210-218 °C

6-Fluoro-2,3-dihydro-3-thioxo-4H-1 ,2,4-benzothiadiazine 1 , 1 -dioxide; mp 246-248 °C The process of preparing the compounds of formula I is further illustrated in the following examples which, however, are not to be construed as limiting.

General procedure for the preparation of 3-methylsulfanyl-4H-1 ,2,4-benzothiadiazine 1 , 1 -dioxides

The appropriate 3-thioxo-2,3-dihydro-4H-1 ,2,4-benzothiadiazine 1 , 1 -dioxide (0.05 mol) was dissolved in a mixture of aqueous 2.5% w/v sodium hydrogen carbonate (280mL) and methanol (280 mL) and supplemented with an excess of methyl iodide (0.35 mol). After stirring for 30-60 min (until completion of the reaction monitored by t.l.c), the resulting suspension was adjusted to pH 6. The suspension was concentrated to a volume of 300 mL by distillation under reduced pressure. The precipitate was collected by filtration, washed with water and dried (yields: 80-95%). In this way the following five compounds were prepared:

EXAMPLE 1

7-lodo-3-methylsulfanyl-4H-1 ,2,4-benzothiadiazine 1 , 1 -dioxide mp 271 -273 °C.

EXAMPLE 2

7-Fluoro-3-methylsulf anyl-4H-1 ,2,4-benzothiadiazine 1 , 1 -dioxide mp 265-268 °C.

EXAMPLE 3

7-Methyl-3-methylsulfanyl-4H-1 ,2,4-benzothiadiazine 1 ,1 -dioxide mp 275-278 °C

EXAMPLE 4

7-Methoxy-3-methylsulfanyl-4H-1 ,2,4-benzothiadiazine 1 , 1 -dioxide mp 270-276 °C.

EXAMPLE 5

5-Chloro-3-methylsulfanyl-4H-1 ,2,4-benzothiadiazine 1 , 1 -dioxide mp 208-210 °C.

EXAMPLE 6

7-Chloro-3-cyclopropylmethylsulfanyl-4H-1 ,2,4-benzothiadiazine 1 , 1 -dioxide Sodium bicarbonate (84mg, 1 mmol) was added to a solution of 7-chloro-2H-1,2,4- benzothiadiazine-3(4H)-thione 1,1 -dioxide (249 mg, 1 mmol) and bromomethylcyclo- propane (135 mg,1 mmol) in dry DMF (2 ml) . The reaction mixture was stirred for 48 h at 60 °C and concentrated in vacuo. The residue was treated with water (2 ml) and the solid was collected by filtration and dried giving 130 mg (43%) of the title compound; mp 214-215 °C, 1H-NMR (d6-DMSO): 0.36 (m, 2H), 0.57 (m, 2H), 1.13 (m,1H), 3.09 (d, 2H), 7.29 (d, 1H), 7.75 (dd, 1H), 7.84 (d, 1H), 12.65 (s, 1H).

EXAMPLE 7

7-Chloro-3-(3-trifluoromethylbenzylsulfanyl)-4H-1 ,2,4-benzothiadiazine 1 , 1 -dioxide By following a procedure analogous to the one described in EXAMPLE 6, 3- trifluoromethylbenzyl bromide (239 mg,1 mmol) was treated with 7-chloro-2H-1,2,4- benzothiadiazine-3(4H)-thione 1,1 -dioxide (249 mg,1 mmol) to give 110 mg (27.4%) of the title compound; mp >220 °C, 1 H-NMR (d6-DMSO): 3.0 (t, 2H), 3.75 (q, 2H), 7.41 (d, 2H), 7.89 (s,1H), 7.95 (s, 1H), 8.05 (s, 2H), 8.62 (d, 2H), 9.5 (s, 1H).

EXAMPLE 8

7-Chloro-3-(3-methyl-but-2-enylsulfanyl)-4H-1,2,4-benzothiadiazine 1,1 -dioxide

By following a procedure analogous to the one described in EXAMPLE 6, 3,3- dimethylallyl bromide (149 mg,1 mmol) was treated with 7-chloro-2H- 1,2,4- benzothiadiazine-3(4H)-thione 1,1-dioxide (249 mg,1 mmol) to give 90 mg (28.5%) of the title compound; mp: 170-172 °C, 1 H-NMR (d6-DMSO): 1.68 (2xs, 6H), 3.82 (dd, 2H), 5.32 (m,1H), 7.30 (d, 1H), 7.70 (dd, 1H), 7.83 (d, 1H), 12.65 (s, 1H). General procedure for the preparation of 3-alkoxy-4H-1,2,4-benzothiadiazine 1,1- dioxides

The appropriate 2,3-dihydro-3-oxo-4H-1,2,4-benzothiadiazine 1,1 -dioxide (1.0 g) was dissolved in a solution of NaOH (1.0 equiv.) in methanol (10 mL) and stirred for 10 min. The solvent was removed by distillation under reduced pressure and the residue (sodium salt of the starting compound) was dissolved in DMF (20 mL). The approriate O 99/32467

28

alkyl halide (1 .5 - 2.0 equiv.) was added to the solution and the mixture was heated at 70-80 °C for 4-6 h (until completion of the reaction checked by t.l.c). Two compounds were usually formed: the title compound: 3-alkoxy-4H-1 ,2,4-benzothiadiazine 1 , 1 -dioxide, and the compound of N-alkylation: 2-alkyl-2,3-dihydro-3-oxo-4H-1 ,2,4- benzothiadiazine 1 , 1 -dioxide. The solvent was removed by distillation under reduced pressure and the residue was suspended in distilled water (30 mL). The suspension was adjusted to pH 14 with NaOH 5% w/v in water. The insoluble material was eliminated by filtration and the filtrate was treated with charcoal and filtered. The filtrate was carefully adjusted to pH 10 and the resulting precipitate (essentially the compound of N-alkyiation) was collected by filtration. The filtrate was adjusted to pH 1 and the resulting precipitate (the compound of O-alkylation) was collected by filtration, washed with water and dried.

In this way the following five compounds were prepared:

EXAMPLE 9

7-Fluoro-3-isopropoxy-4H-1 ,2,4-benzothiadiazine 1 , 1 -dioxide monohydrate

The title compound was obtained from 7-fluoro-3-oxo-2,3-dihydro-4H- 1 ,2,4- benzothiadiazine 1 ,1 -dioxide and isopropyl iodide; mp 200-205 °C, IR (KBr): 3594, 3532, 2988, 1591 , 1543, 1499, 1317, 1287, 1260, 1 167, 1092 cm-1 .

EXAMPLE 10

3-Cyclopropylmethoxy-7-fluoro-4H-1 ,2,4-benzothiadiazine 1 , 1 -dioxide hemihydrate

The title compound was obtained from 7-fluoro-3-oxo-2,3-dihydro-4H-1 ,2,4- benzothiadiazine 1 , 1 -dioxide and cyclopropylmethyl bromide; mp 1 53-1 56 °C, IR (KBr- ): 3478, 3249, 1618, 1584, 1538, 1494, 1368, 1314, 1256, 1 159 cm-1 EXAMPLE 11

5 3-lsopropoxy-7-methyl-4H-1,2,4-benzothiadiazine 1,1 -dioxide monohydrate

The title compound was obtained from 7-methyl-3-oxo-2,3-dihydro-4H-1,2,4- benzothiadiazine 1,1 -dioxide and isopropyl iodide; mp212-215 °C, IR (KBr): 3574, 3519, 2984, 1589, 1532, 1501 , 1311, 1281 , 1265, 1169 cm-1. 0

EXAMPLE 12

3-lsopropoxy-7-methoxy-4H-1 ,2,4-benzothiadiazine 1 , 1 -dioxide monohydrate 15

The title compound was obtained from 7-methoxy-3-oxo-2,3-dihydro-4H- 1,2,4- benzothiadiazine 1,1 -dioxide and isopropyl iodide; mp 162-176 °C, IR (KBr): 3570, 3513, 3053, 2983, 1586, 1541, 1504, 1318, 1279, 1170, 1095 cm-1.

20

EXAMPLE 13

7-Chloro-3-cyclopentyloxy-4H-1 ,2,4-benzothiadiazine 1 , 1 -dioxide

25 The title compound was obtained from 7-chloro-3-oxo-2,3-dihydro-4H-1,2,4- benzothiadiazine 1,1 -dioxide and cyclopentyl bromide. The compound was purified by refiuxing in ethyl acetate for 20 min. The suspension was cooled and the insoluble material was collected by filtration, washed with ethyl acetate and dried; mp >300 °C, IR (KBr): 3253, 3188, 3104, 2952, 2875, 1617, 1601, 1580, 1521, 1480,

30 1337, 1297, 1252, 1158, 1104 cm-1.

General procedure for the preparation of 3-alkylsulfanyl-4H-1,2,4-benzothiadiazine 1,1 -dioxides The appropriate 2,3-dihydro-3-thioxo-4H-1,2,4-benzothiadiazine 1,1 -dioxide (0.5 g) was dissolved (or suspended) in a mixture of acetonitrile (13 mL) and DMF (1 mL) and then supplemented with anhydrous potassium carbonate (0.5 g) and an excess of the appropriate alkyl halide (1.0 - 1.5 mL). The suspension was stirred at room temperature for 24 - 72 h (until completion of the reaction checked by t.l.c). The solvent and the excess of the reagent were removed by distillation under reduced pressure and the residue was dissolved in a dilute (1-2%) aqueous or hydromethanolic 1:1 solution of NaOH (10-20 mL). The solution was treated with charcoal, filtered off, and the filtrate was adjusted to pH 5-6. The resulting precipitate was collected by filtration, washed with water and dried.

In this way the following seventeen compounds were prepared:

EXAMPLE 14

7-Fluoro-3-ethylsulfanyl-4H-1,2,4-benzothiadiazine 1,1 -dioxide monohydrate

The title compound was obtained from 7-fluoro-3-thioxo-2,3-dihydro-4H-1,2,4- benzothiadiazine 1,1 -dioxide and ethyl bromide; mp 205-208 °C, IR (KBr): 3603, 3536, 3078, 3056, 2980, 2946, 1634, 1609, 1564, 1527, 1494, 1287, 1268, 1233, 1197, 1156, 1134 cm-1.

EXAMPLE 15

7-Fluoro-3-isopropyisulfanyl-4H-1,2,4-benzothiadiazine 1,1 -dioxide hemihydrate

The title compound was obtained from 7-fluoro-3-thioxo-2,3-dihydro-4H-1,2,4- benzothiadiazine 1,1 -dioxide and isopropyl iodide; mp 190-193 °C, IR (KBr): 3580, 3517, 2976, 2932, 1563, 1525, 1492, 1291, 1266, 1224, 1193, 1156, 1134 cm-1. EXAMPLE 16

3-Cyclopropylmethylsulfanyl-7-f luoro-4H-1 ,2,4-benzothiadiazine 1 , 1 -dioxide

The title compound was obtained from 7-fluoro-3-thioxo-2,3-dihydro-4H-1,2,4- benzothiadiazine 1,1 -dioxide and cyclopropylmethyl bromide; mp 218-224 °C, IR (KBr): 3237, 3073, 1552, 1521, 1487, 1303, 1260, 1224, 1193, 1150, 1130 cm-1.

EXAMPLE 17

7<Chloro-3-ethylsulfanyl-4H-1,2,4-benzothiadiazine 1,1 -dioxide

The title compound was obtained from 7-chloro-3-thioxo-2,3-dihydro-4H-1,2,4- benzothiadiazine 1,1-dioxide and ethyl bromide; mp 252-255 °C, IR (KBr): 3233, 3186, 3090, 1605, 1555, 1516, 1477, 1294, 1254, 1203, 1156, 1143, 1108 cm-1,

EXAMPLE 18

7-Bromo-3-ethylsulfanyl-4H-1,2,4-benzothiadiazine 1,1 -dioxide

The title compound was obtained from 7-bromo-3-thioxo-2,3-dihydro-4H-1,2,4- benzothiadiazine 1,1-dioxide and ethyl bromide; mp 277-278 °C, IR (KBr): 3234,

3184, 3084, 1608, 1598, 1552, 1513, 1478, 1293, 1252, 1202, 1156, 1144, 1092 cm-1.

EXAMPLE 19

7-Bromo-3-isopropylsulfanyl-4H-1,2,4-benzothiadiazine 1,1-dioxide The title compound was obtained from 7-bromo-3-thioxo-2,3-dihydro-4H-1,2,4- benzothiadiazine 1,1-dioxide and isopropyl iodide; mp 240-246 °C, IR (KBr): 3237, 3186, 3089, 1608, 1597, 1552, 1511, 1476, 1297, 1248, 1201, 1154, 1145, 1091 cm-1.

EXAMPLE 20

7-Bromo-3-cyclopropylmethylsulfanyl-4H-1 ,2,4-benzothiadiazine 1 , 1 -dioxide

The title compound was obtained from 7-bromo-3-thioxo-2,3-dihydro-4H-1,2,4- benzothiadiazine 1,1 -dioxide and cyclopropylmethyl bromide; mp 242-244 °C, IR (KBr): 3233, 3183, 3088, 3012, 1607, 1598, 1553, 1517, 1478, 1296, 1253, 1201, 1157, 1146, 1091 cm-1.

EXAMPLE 21

6-Fluoro-3-ethylsulfanyl-4H-1,2,4-benzothiadiazine 1,1 -dioxide

The title compound was obtained from 6-fiuoro-3-thioxo-2,3-dihydro-4H-1,2,4- benzothiadiazine 1,1 -dioxide and ethyl bromide; mp 218-220 °C, IR (KBr): 3238, 3200, 3153, 3107, 3081, 1617, 1558, 1477, 1297, 1268, 1206, 1154, 1121 cm-1.

EXAMPLE 22

3-Cyclopropylmethylsulfanyl-6-fluoro-4H-1 ,2,4-benzothiadiazine 1 , 1 -dioxide

The title compound was obtained from 6-fluoro-3-thioxo-2,3-dihydro-4H-1,2,4- benzothiadiazine 1,1-dioxide and cyclopropylmethyl bromide; mp 208-211 °C, IR (KBr): 3237, 3200, 3155, 3104, 3075, 1616, 1557, 1478, 1301, 1208, 1155, 1121 cm-1. EXAMPLE 23

6-Chloro-3-ethylsulfanyl-4H-1,2,4-benzothiadiazine 1,1 -dioxide

The title compound was obtained from 6-chloro-3-thioxo-2,3-dihydro-4H-1,2,4- benzothiadiazine 1,1 -dioxide and ethyl bromide; mp 233-240 °C, IR (KBr): 3230, 3180, 3099, 3068, 1605, 1595, 1557, 1471, 1297, 1197, 1160, 1138, 1096 cm-1.

EXAMPLE 24

6-Chloro-3-isopropylsulf anyl-4H- 1 ,2,4-benzothiadiazine 1 , 1 -dioxide

The title compound was obtained from 6-chloro-3-thioxo-2,3-dihydro-4H-1,2,4- benzothiadiazine 1,1 -dioxide and isopropyl iodide; mp 249-253 °C, IR (KBr): 3251, 3082, 2967, 1606, 1553, 1466, 1300, 1198, 1157, 1136, 1090 cm-1.

EXAMPLE 25

6-Chloro-3-cyclopropylmethylsulfanyl-4H-1 ,2,4-benzothiadiazine 1 , 1 -dioxide

The title compound was obtained from 6-chloro-3-thioxo-2,3-dihydro-4H-1,2,4- benzothiadiazine 1,1-dioxide and cyclopropylmethyl bromide; mp 212-217 °C, IR (KBr): 3232, 3179, 3097, 3064, 1594, 1555_> 1471, 1303, 1196, 1160, 1137, 1095 cm-1.

EXAMPLE 26

6-Chloro-3-cyclobutylsulfanyl-4H-1,2,4-benzothiadiazine 1,1-dioxide The title compound was obtained from 6-chloro-3-thioxo-2,3-dihydro-4H-1,2,4- benzothiadiazine 1,1-dioxide and cyclobutyl bromide; mp 251-254 °C, IR (KBr): 3224, 3173, 3064, 2984, 1606, 1552, 1463, 1300, 1196, 1157, 1121, 1088 cm-1.

EXAMPLE 27

6-Bromo-3-ethylsulfanyl-4H-1 ,2,4-benzothiadiazine 1 , 1 -dioxide

The title compound was obtained from β-bromo-3-thioxo-2,3-dihydro-4H-1,2,4- benzothiadiazine 1,1 -dioxide and ethyl bromide; mp 269-273 °C, IR (KBr): 3232, 3177, 3078, 3056, 2984, 1603, 1557, 1518, 1465, 1293, 1202, 1159, 1140, 1082 cm-1.

EXAMPLE 28

6-Bromo-3-isopropylsulfanyl-4H-1 ,2,4-benzothiadiazine 1 , 1 -dioxide

The title compound was obtained from 6-bromo-3-thioxo-2,3-dihydro-4H-1,2,4- benzothiadiazine 1,1 -dioxide and isopropyl iodide; mp 244-252 °C, IR (KBr): 3239, 3178, 3073, 2970, 2927, 1597, 1552, 1465, 1291, 1198, 1163, 1137, 1082 cm-1.

EXAMPLE 29

6-Bromo-3-cyclobutylsulfanyl-4H-1 ,2,4-benzothiadiazine 1 , 1 -dioxide

The title compound was obtained from 6-bromo-3-thioxo-2,3-dihydro-4H-1,2,4- benzothiadiazine 1,1 -dioxide and cyclobutyl bromide; mp 265-270 °C, IR (KBr): 3224, 3168, 3071, 2980, 1592, 1548, 1460, 1300, 1196, 1157, 1119, 1077 cm-1. EXAMPLE 30

6,7-Dichloro-3-isopropylsulfanyl-4H-1 ,2,4-benzothiadiazine 1 , 1 -dioxide

The title compound was obtained from 6,7-dichloro-3-thioxo-2,3-dihydro-4H-1 ,2,4- benzothiadiazine 1 ,1 -dioxide and isopropyl iodide; m.p.: > 300°C, IR (KBr): 3252, 3183, 3089, 1612, 1557, 1459, 1303, 1286, 1 160 cm-1 .

General procedure for the preparation of 3-alkylsulfinyl-4H-1 ,2,4-benzothiadiazine 1 , 1 - dioxides

The appropriate 3-alkylsulfanyl*4H-1 ,2,4-benzothiadiazine 1 ,1 -dioxide (1 .0 mmol) was suspended in distilled water (25 mL) and supplemented with sodium carbonate (1 .1 mmol) and a few drops of dilute NaOH until complete dissolution. Bromine (1 .1 mmol) was then added under vigorous stirring and the resulting suspension was stirred for 30 min. at room temperature. The suspension was adjusted to pH 4-5 and the insoluble material was collected by filtration, washed with water and dried. The crude compound was recrystallized in the appropriate solvent.

In this way the following compound was prepared:

EXAMPLE 31

7-Chloro-3-isopropylsulfinyl-4H-1 ,2,4-benzothiadiazine 1 ,1 -dioxide

The title compound was obtained from the reaction of 7-chloro-3-isopropylsulfanyl-4H- 1 ,2,4-benzothiadiazine 1 , 1 -dioxide with bromine in alkaline medium as described above. The crude compound was purified by stirring in methanol. The insoluble material was collected by filtration and suspended in diethylether (two fold). The insoluble compound was collected by filtration, washed with diethylether and dried; mp 257-260 °C, IR (KBr): 3148, 2977, 1 606, 1 570, 1 507, 1477, 1 326, 1 173, 1 1 10, 1060, 1028 cm-1 . EXAMPLE 32

7-Chloro-3-cyclopentyloxy-4H-1.2.4-benzothiadiazine 1 ,1 -dioxide 5 A solution of 7-chloro-2H-1,2,4-benzothiadiazin-3(4H)-one 1,1 -dioxide sodium salt (0.75 g), cyclopentyl bromide (1.55 ml), and potassium tert-butoxide (0.17 g) in dry DMF (3 ml) was heated at 55 - 60 °C for 48 h. The solvent was evaporated and the residue was triturated with 25 ml of water. The precipitate was collected by filtration, 0 washed with water and dried. Recrystallization from methanol gave the title compound as white crystals; mp 332 - 34 °C, ¹H-NMR(DMSO-d₆) δ (ppm): 12.20 (br, 1H), 7.82 (d, J = 2 Hz, 1H), 7.70 (dd, 1H), 7.29 (d, J = 9 Hz, 1H), 5.41 - 5.28 (m, 1H), -2.1 - 1.5 (m, 8H).

15 EXAMPLE 33

7-Chloro-3-(5-chloro-2-methoxybenzyloxy)-4H-1.2.4-benzothiadiazine 1.1 -dioxide

The title compound was prepared from 7-chloro-2H-1,2,4-benzothiadiazin-3(4H)-one 20 1,1 -dioxide sodium salt and 5-chloro-2-methoxybenzyl chloride by a procedure analogous to the procedure described in example 32; 'H-NMRfDMSO-dg) δ (ppm): 12.40 (s, 1H), 7.85 (d, J = 2 Hz, 1H), 7.71 (dd, 1H), 7.55 (d, J = 2 Hz, 1H), 7.46 (dd, 1H), 7.28 (d, J = 6 Hz, 1H), 7.11 (d, J = 6 Hz, 1H), 5.32 (s, 2H), 3.83 (s, 3H), IR(KBr) v [cm¹] = 3237, 3175, 3104, 3043, 2941, 2844, 1621, 1601, 1581, 1486, 25 1400, 1330, 1298, 1254, 1167, 1128, 1107, 1017.

EXAMPLE 34

7-Chloro-3-cyclopropylmethoxv-4H-1.2.4-benzothiadiazine 1.1 -dioxide 30

The title compound was prepared from 7-chloro-2H-1,2,4-benzothiadiazin-3(4H)-one 1,1 -dioxide sodium salt and cyclopropylmethyl bromide by a procedure analogous to the procedure described in example 32; 'H-MRfDMSO-dg) δ (ppm): 12.35 (br, 1H), 7.82 (d, J = 2Hz), 7.71 (dd, 1H), 7.29 (d, J = 9 Hz, 1H), 4.18 (d, J = 7 Hz), 1.35 1.13 (m, 1H), 0.68 - 0.35 (m, 4H), IR(KBr) v [cm¹] = 3251, 3187, 3107, 3029, 1619, 1602, 1583, 1525, 1480, 1387, 1353, 1297, 1252, 1162, 1107, 974.

Claims

O 99/32467 38 CLAIMS

1. A compound of the general formula

wherein

Z is O, S, S(=0), S(=O)_2l S(=NR), S(=0)(=NR) or S(=NR)₂

wherein R is hydrogen; C,.₆-alkyl, C₂.₆-alkenyl or C^-alkynyl optionally mono- or polysubstituted with halogen, hydroxy or C_1-6-alkoxy; or C-j-g-cycloalkyl optionally mono- or polysubstituted with C.,.₆-alkyl, halogen, hydroxy or C,.₆-alkoxy;

R³ is Ca-g-cycloalkyl or (C₃.₆-cycloalkyl)C.|.₆-alkyl the C^-cycloalkyl group optionally being mono- or polysubstituted with C^-alky!, halogen, hydroxy or C_1-6-alkoxy; a 3-6 membered saturated ring system comprising one or more nitrogen-, oxygen- or sulfur atoms, optionally being mono- or polysubstituted with halogen, cyano, trifluoromethyl, C^-alky!, C_1-6-alkoxy, C₁.₆-alkoxy-Cι.₆-alkyl, aryl, arylalkyl, hydroxy, oxo, nitro, amino, C,.₆-monoalkyl or dialkylamino; or straight or branched C^-alky!, C₂.₁₈-alkenyl or C₂.₁₈-alkynyl, each of the groups being optionally mono- or polysubstituted with halogen, hydroxy, C_1-6-alkoxy, C-,.₆- alkylthio,

nitro, amino, C_1-6- monoalkyl- or dialkylamino, cyano, oxo, formyl, acyl, carboxy, C,.₆-alkoxycarbonyl, carbamoyl, formylamino, or C^-alkylcarbonylamino, aryl, aryioxy, arylalkoxy, the aryl group optionally being mono- or polysubstituted with C_halky!, perhalomethyl, halogen, hydroxy or C^-alkoxy; bicycloalkyl, aryl, heteroaryl, arylalkyl or heteroarylalkyl, each of the groups being optionally mono- or polysubstituted with halogen, hydroxy, C,.₆-alkyl, C_1-6-alkoxy, aryioxy, arylalkoxy, nitro, amino, C^- monoalkyl- or dialkylamino, cyano, oxo, acyl or C_1-6-alkoxycarbonyl;

or R³ is

wherein n, m and p independently are 0, 1 , 2 or 3 and R¹⁰ is hydrogen; hydroxy; C,.₆- alkoxy; Q-j-β-cycloalkyl optionally mono- or polysubstituted with C_1-6-alkyl, halogen, hydroxy or C_1-6-alkoxy; C_1-6-alkyl, C₂.₆-alkenyl or C₂.₆-alkynyl optionally mono- or polysubstituted with halogen;

R⁵, R⁶, R⁷, R⁸ independently are hydrogen, halogen; C,.₁₈-alkyl; C-₃.₆-cycloalkyl; hydroxy; C,. ₆-alkoxy; C₁.₆-alkoxy-C₁.₆-alkyl; nitro; amino; cyano; cyanomethyl; perhalomethyl; C-,^- monoalkyl- or dialkylamino; sulfamoyl; C^-alkylthio; C^-alkylsulfonyl; C^-alkylsulfinyl; C,. ₆-alkylcarbonylamino; arylthio, arylsulfinyl, arylsuifonyl, aryl, arylalkyl, aryioxy, the aryl group optionally being mono- or polysubstituted with C_1-6-alkyl, perhalomethyl, halogen, hydroxy or C_1-6-alkoxy; C_1-6-alkoxycarbonyl; C₁.₆-alkoxycarbonyl-C_1-6-alkyl; carbamyl; carbamylmethyl; C,.₆-monoalkyl- or dialkylaminocarbonyl; C_Ls-monoalkyl- or dialkylami- nothiocarbonyl; ureido; C^-monoalkyl- or dialkylaminocarbonylamino, thiocarbamyl; thioureido; C-,.₆-monoalkyl- or dialkylaminothiocarbonylamino; C_1-6-monoalkyl- or dialky- laminosulfonyl; carboxy; carboxy-C_1-6-alkyl; acyl; formyl; or a 5 - 6 membered nitrogen, oxygen or sulfur containing ring, optionally substituted with C^-alky! or phenyl, the phenyl group optionally being mono- or polysubstituted with

perhalomethyl, halogen, hydroxy or C^-alkoxy; or a salt thereof with a pharmaceutically acceptable acid or base, or any optical isomer or mixture of optical isomers, including a racemic mixture, or any tautomeric form.

2. A compound according to claim 1 , wherein Z is S.

3. A compound according to claim 1 or 2 wherein one of R⁵, R⁶, R⁷ or R⁸ is halogen.

4. A compound according to anyone of the preceding claims wherein R⁷ is chloro.

5. A compound according to anyone of the preceding claims wherein R³ is straight or branched C_1-18 -alkyl,

or (C_M-cycloalkyl)C,-_β-alkyl.

6. A compound selected from the following:

7-chloro-3-isobutylsulfanyl-4H-1 ,2,4-benzothiadiazine 1 , 1 -dioxide 7-chloro-3-cyclobutylsulfanyl-4H-1 ,2,4-benzothiadiazine 1 ,1 -dioxide 7-chloro-3-cyclopentylsulfanyl-4H-1 ,2,4-benzothiadiazine 1 , 1 -dioxide 7-chloro-3-(1 -phenylethyl)sulfanyl-4H-1 ,2,4-benzothiadiazine 1 , 1 -dioxide 7-bromo-3-isopropylsulfany!-4H-1 ,2,4-benzothiadiazine 1 ,1 -dioxide 7-fluoro-3-isopropylsulfanyl-4H-1 ,2,4-benzothiadiazine 1 , 1 -dioxide 6-fluoro-3-isopropylsulfanyl-4H-1 ,2,4-benzothiadiazine 1 ,1 -dioxide 6,8-dichloro-3-isopropylsulfanyl-4H-1 ,2,4-benzothiadiazine 1 ,1 -dioxide 6,7-dichloro-3-isopropylsulfanyl-4H-1 ,2,4-benzothiadiazine 1 ,1 -dioxide 6-methoxy-3-isopropy!sulfanyl-4H-1 ,2,4-benzothiadiazine 1 ,1 -dioxide 7-methoxy-3-isopropylsulfanyl-4H-1 ,2,4-benzothiadiazine 1 , 1 -dioxide 7-trifluoromethyl-3-isopropylsulfanyl-4H-1 ,2,4-benzothiadiazine 1 , 1 -dioxide 6-trifluoromethyl-3-isopropylsulfanyl-4H-1 ,2,4-benzothiadiazine 1 ,1 -dioxide 7-chloro-3-ethylsulfinyl-4H-1 ,2,4-benzothiadiazine 1 , 1 -dioxide 7-chloro-3-propylsulfinyl-4H-1 ,2,4-benzothiadiazine 1 ,1 -dioxide 7-chloro-3-isopropylsulfinyl-4H-1 ,2,4-benzothiadiazine 1 ,1 -dioxide 7-chloro-3-ethylsulfinimidoyl-4H-1 ,2,4-benzothiadiazine 1 ,1 -dioxide 6-fluoro-3-ethylsulfinimidoyl-4H-1 ,2,4-benzothiadiazine 1 ,1 -dioxide 7-chloro-3-ethylsulfonimidoyl-4H-1,2,4-benzothiadiazine 1 ,1 -dioxide 7-bromo-3-isopropoxy-4H-1 ,2,4-benzothiadiazine 1 ,1 -dioxide 7-fluoro-3-isopropoxy-4H-1 ,2,4-benzothiadiazine 1 , 1 -dioxide 6-fluoro-3-isopropoxy-4H-1 ,2,4-benzothiadiazine 1 , 1 -dioxide ,8-dichloro-3-isopropoxy-4H-1 ,2,4-benzothiadiazine 1 , 1 -dioxide -isopropoxy-6-methoxy-4H-1 ,2,4-benzothiadiazine 1 , 1 -dioxide -isopropoxy-7-methoxy-4H-1 ,2,4-benzothiadiazine 1 ,1 -dioxide -isopropoxy-7-trifluoromethyl-4H-1 ,2,4-benzothiadiazine 1 ,1 -dioxide -chloro-3-cyclopropylmethylsulfanyl-4H-1 ,2,4-benzothiadiazine 1 , 1 -dioxide -chloro-3- cyclopropylmethoxy-4H-1 ,2,4-benzothiadiazine 1 ,1 -dioxide -Chloro-3-(3-trifluoromethylbenzylsulfanyl)-4H-1 ,2,4-benzothiadiazine 1 , 1 -dioxide -Chloro-3-(3-methyl-but-2-enylsulfanyl)-4H-1 ,2,4-benzothiadiazine 1 ,1 -dioxide -bromo-3-isopropoxy-4H-1 ,2,4-benzothiadiazine 1,1 -dioxide -bromo-3-isopropylsulfanyl-4H-1 ,2,4-benzothiadiazine 1 , 1 -dioxide -bromo-3-cyclopropylmethylsulfanyl-4H-1,2,4-benzothiadiazine 1 ,1 -dioxide -bromo-3-cyclopropylmethoxy-4H-1 ,2,4-benzothiadiazine 1 , 1 -dioxide -bromo-3-isobutylsulfanyl-4H-1 ,2,4-benzothiadiazine 1 , 1 -dioxide -bromo-3-cyclobutylsulfanyl-4H-1 ,2,4-benzothiadiazine 1 ,1 -dioxide 6-bromo-3-cyclopentylsulfanyl-4H-1 ,2,4-benzothiadiazine 1 ,1 -dioxide 6-bromo-3-(1-phenylethyl)sulfanyl-4H-1 ,2,4-benzothiadiazine 1 ,1 -dioxide 3-isopropoxy-7-methyl-4H-1 ,2,4-benzothiadiazine 1 , 1 -dioxide 3-isopropylsulfanyl-7-methyl-4H-1 ,2,4-benzothiadiazine 1 ,1 -dioxide 3-cyclopropylmethylsulfanyl-7-methyl-4H-1 ,2,4-benzothiadiazine 1 , 1 -dioxide 3-cyclopropylmethoxy-7-methyl-4H-1 ,2,4-benzothiadiazine 1 ,1 -dioxide 3-isobutylsulfanyl-7-methyl-4H-1 ,2,4-benzothiadiazine 1 ,1 -dioxide 3-cyclobutylsulfanyl-7-methyl-4H-1 ,2,4-benzothiadiazine 1 , 1 -dioxide 3-cyclopentylsulfanyl-7-methyl-4H-1 ,2,4-benzothiadiazine 1 ,1 -dioxide 3-(1-phenylethyl)sulfanyl-7-methyl-4H-1 ,2,4-benzothiadiazine 1 ,1 -dioxide 3-cyclopropylmethoxy-7-fluoro-4H-1 ,2,4-benzothiadiazine 1 ,1-dioxide7-chloro-3- cyclopentyloxy-4H-1 ,2,4-benzothiadiazine 1 , 1 -dioxide7-fluoro-3-ethylsulfanyl-4H- 1 ,2,4-benzothiadiazine 1 ,1 -dioxide7-fluoro-3-cyclopropylmethylsulfanyl-4H-1 ,2,4- benzothiadiazine 1 , 1 -dioxide7-chloro-3-ethylsulf anyl-4H-1 ,2,4-benzothiadiazine 1 ,1- dioxide7-bromo-3-ethylsulfanyl-4H-1 ,2,4-benzothiadiazine 1 ,1 -dioxide7-bromo-3- cyclopropylmethylsulfanyl-4H-1 ,2,4-benzothiadiazine 1 , 1-dioxide3-ethylsulfanyl-6- fluoro-4H-1 ,2,4-benzothiadiazine 1 , 1 -dioxide3-cyclopropylmethylsulfanyl-6-fluoro-4H- 1 ,2,4-benzothiadiazine 1 , 1 -dioxide6-chloro-3-ethylsulfanyl-4H-1 ,2,4-benzothiadiazine 1 , 1 -dioxide6-chloro-3-isopropylsuif anyl-4H-1 ,2,4-benzothiadiazine 1 , 1 -dioxideδ-chloro- 3-cyclopropylmethylsulfanyl-4H-1 ,2,4-benzothiadiazine 1 , 1 -dioxide6-chloro-3- cyclobutylsulfanyl-4H-1 ,2,4-benzothiadiazine 1 ,1 -dioxide6-bromo-3-ethylsulfanyl-4H- 1 ,2,4-benzothiadiazine 1 , 1 -dioxide7-chloro-3-(5-chloro-2-methoxybenzyloxy)-4H-1 ,2,4- benzothiadiazine 1 , 1 -dioxide7-chloro-3-cyclobutoxy-4H-1 ,2,4-benzothiadiazine 1 ,1 - dioxide7-chloro-3-(1 -phenyl)ethoxy-4H-1 ,2,4-benzothiadiazine 1 ,1 -dioxide

7. Compounds according to any one of the preceding claims which acts as openers of the K_ATP-regulated potassium channels.

8. A method of preparing a compound of formula I, characterized in

a) reacting a compound of formula II:

R³-X (III)

in the presence of a base, wherein R³ is as defined above and X is a leaving group selected from sulfate, chloro, bromo or iodo to form a compound of the general formula I wherein Z is O or S, or b) reacting a compound of formula II:

wherein Y is O and R⁵, R⁶ , R⁷ and R⁸ are as defined above with a diazo compound of 5 formula IV

R'R"CN₂ (IV)

o wherein R' and R" together as two substituents on methyl form a group R'R"CH meeting the criteria defined above for R³, to form a compound of the general formula I wherein Z is O and R³ is R'R"CH, or

c) reacting a compound of formula V: 5

wherein R⁵, R⁶ , R⁷ and R⁸ are as defined above and Q is a leaving group selected from chloro, bromo, iodo, amino, trimethylamino, imidazol-1-yl, methylsulfanyl, methylsulfinyl 0 or methylsulfonyl with a compound of formula VI:

R³YH (VI)

in the presence of a base, wherein R³ is as defined above and Y is O or S to form a 5 compound of the general formula I wherein Z is O or S, or d) reacting a compound of formula VII:

wherein R³, R⁵, R⁶ , R⁷ and R⁸ are as defined above with an oxidizing agent to form a compound of the general formula I wherein Z is S(=0) or S(=0)₂, or

e) reacting a compound of formula VII:

wherein R³, R⁵, R⁶ , R⁷ and R⁸ are as defined above with an aminating agent, to form a compound of the general formula VIII

wherein n is 1 or 2, or

f) reacting a compound of formula VII:

wherein R³, R⁵, R⁶ , R⁷ and R⁸ are as defined above with an aminating agent and subse- quently an oxidizing agent, or vice versa, to form a compound of the general formula I wherein Z is S(=0)(=NR), or

g) reacting a compound of formula IX

R³-X (III)

wherein R³ is as defined above and X is a leaving group selected from sulfate, chloro, bromo or iodo to form a compound of formula X

which by ring-closure forms a compound of the general formula I, or 5 h) reacting a compound of formula XI

1 o wherein R³, R⁵, R⁶, R⁷ and R⁸ are as defined above and PG is a protecting group selected from substituted benzyl, with chlorosulfonyl isocyanate (CI-S0₂-NCO) and subsequent ring closure folllowed by removal of the protecting group to form a compound of formula I.

9. A pharmaceutical composition comprising a compound according to any of the

15 claim 1 - 6 or a pharmaceutical acceptable salt thereof with a pharmaceutically acceptable acid or base, or any optical isomer or mixture of optical isomers, including a racemic mixture, or any tautomeric form together with one or more pharmaceutically acceptable carriers or diluents.

20 10. A pharmaceutical composition for use in the treatment of diseases of the endocrinological system such as hyperinsulinaemia and diabetes comprising a compound according to any of the claims 1 - 6 or a pharmaceutical acceptable salt thereof with a pharmaceutically acceptable acid or base, or any optical isomer or mixture of optical isomers, including a racemic mixture, or any tautomeric form together with one or more

25 pharmaceutically acceptable carriers or diluents.

11. The pharmaceutical composition according to claim 9 or 10 in the form of an oral dosage unit or parenteral dosage unit.

12. A pharmaceutical composition according to claim 9 or 10 wherein said compound is administered as a dose in a range from about 0.05 to 1000, preferably from about 0.1 to

500 and especially in the range from 50 to 200 mg per day.

13. A compound according to any one of the claims 1 - 6 or a pharmaceutically acceptable salt thereof with a pharmaceutically acceptable acid or base, or any optical isomer or mixture of optical isomers, including a racemic mixture, or any tautomeric form for therapeutical use.

14. A compound according to any one of the claims 1 - 6 or a pharmaceutically acceptable salt thereof with a pharmaceutically acceptable acid or base, or any optical isomer or mixture of optical isomers, including a racemic mixture, or any tautomeric form for therapeutical use in the treatment or prevention of diseases of the endocrinological system, such as hyperinsulinaemia and diabetes.

15. The use of a compound according to any one of the claims 1 - 6 or a pharmaceutically acceptable salt thereof with a pharmaceutically acceptable acid or base, or any optical isomer or mixture of optical isomers, including a racemic mixture, or any tautomeric form as a medicament.

16. The use of a compound according to any of the claims 1 - 6 for preparing a medicament.

17. The use of a compound according to any one of the claims 1 - 6 or a pharmaceutically acceptable salt thereof with a pharmaceutically acceptable acid or base, or any optical isomer or mixture of optical isomers, including a racemic mixture, or any tautomeric form for the preparation of a medicament for the treatment or prevention of diseases of the endocrinological system, such as hyperinsulinaemia and diabetes.

18. A method of treating or preventing diseases of the endocrinological system, such as hyperinsulinaemia and diabetes in a subject in need thereof comprising administering an effective amount of a compound according to any of the claims 1 - 6 to said subject.

19. A process for the manufacture of a medicament, particular to be used in the 5 treatment or prevention of diseases of the endocrinological system, such as hyperinsulinaemia and diabetes which process comprising bringing a compound of formula I according to any of the claims 1 - 6 or a pharmaceutically acceptable salt thereof into a galenic dosage form.

10 20. Any novel feature or combination of features as described herein.