DOP2013000308A - N-(6-((2r,3s)-3,4-dihidroxibutan-2-iloxi)-2-(4-fluorobenciltio)pirimidin-4-il)-3-metilacetidina-1-sulfonamida como modulador del receptor de quimiocina - Google Patents
N-(6-((2r,3s)-3,4-dihidroxibutan-2-iloxi)-2-(4-fluorobenciltio)pirimidin-4-il)-3-metilacetidina-1-sulfonamida como modulador del receptor de quimiocinaInfo
- Publication number
- DOP2013000308A DOP2013000308A DO2013000308A DO2013000308A DOP2013000308A DO P2013000308 A DOP2013000308 A DO P2013000308A DO 2013000308 A DO2013000308 A DO 2013000308A DO 2013000308 A DO2013000308 A DO 2013000308A DO P2013000308 A DOP2013000308 A DO P2013000308A
- Authority
- DO
- Dominican Republic
- Prior art keywords
- compound
- methylacetidine
- fluorobencilti
- dihydroxibutan
- chemiocine
- Prior art date
Links
- 229940124530 sulfonamide Drugs 0.000 title abstract 2
- 229940075993 receptor modulator Drugs 0.000 title 1
- 150000001875 compounds Chemical class 0.000 abstract 6
- 208000037265 diseases, disorders, signs and symptoms Diseases 0.000 abstract 2
- 102000009410 Chemokine receptor Human genes 0.000 abstract 1
- 108050000299 Chemokine receptor Proteins 0.000 abstract 1
- CZPWVGJYEJSRLH-UHFFFAOYSA-N Pyrimidine Chemical compound C1=CN=CN=C1 CZPWVGJYEJSRLH-UHFFFAOYSA-N 0.000 abstract 1
- 230000009286 beneficial effect Effects 0.000 abstract 1
- 201000010099 disease Diseases 0.000 abstract 1
- 230000000694 effects Effects 0.000 abstract 1
- 238000004519 manufacturing process Methods 0.000 abstract 1
- 238000000034 method Methods 0.000 abstract 1
- 239000008194 pharmaceutical composition Substances 0.000 abstract 1
- 239000012450 pharmaceutical intermediate Substances 0.000 abstract 1
- 150000003839 salts Chemical class 0.000 abstract 1
- 150000003456 sulfonamides Chemical class 0.000 abstract 1
Classifications
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- C07D403/00—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00
- C07D403/02—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00 containing two hetero rings
- C07D403/12—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00 containing two hetero rings linked by a chain containing hetero atoms as chain links
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- A61K31/00—Medicinal preparations containing organic active ingredients
- A61K31/33—Heterocyclic compounds
- A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
- A61K31/495—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with two or more nitrogen atoms as the only ring heteroatoms, e.g. piperazine or tetrazines
- A61K31/505—Pyrimidines; Hydrogenated pyrimidines, e.g. trimethoprim
- A61K31/506—Pyrimidines; Hydrogenated pyrimidines, e.g. trimethoprim not condensed and containing further heterocyclic rings
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- C07C69/92—Esters of carboxylic acids having a carboxyl group bound to a carbon atom of a six-membered aromatic ring of monocyclic hydroxy carboxylic acids, the hydroxy groups and the carboxyl groups of which are bound to carbon atoms of a six-membered aromatic ring with etherified hydroxyl groups
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- C07D239/24—Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings not condensed with other rings having three or more double bonds between ring members or between ring members and non-ring members
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Abstract
Se proporciona un compuesto que es (a) una sulfonamida pirimidina de fórmula (I) o (b) una sal farmacéuticamente aceptable de esta, formas cristalinas del compuesto, procesos para obtener el compuesto, intermediarios farmacéuticos utilizados en la fabricación del compuesto y composiciones farmacéuticas que contienen el compuesto. El compuesto es útil en el tratamiento de una enfermedad/trastorno en donde la modulación de la actividad del receptor de quimiocina es beneficiosa.
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US201161506737P | 2011-07-12 | 2011-07-12 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| DOP2013000308A true DOP2013000308A (es) | 2014-02-28 |
Family
ID=46513787
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| DO2013000308A DOP2013000308A (es) | 2011-07-12 | 2013-12-17 | N-(6-((2r,3s)-3,4-dihidroxibutan-2-iloxi)-2-(4-fluorobenciltio)pirimidin-4-il)-3-metilacetidina-1-sulfonamida como modulador del receptor de quimiocina |
Country Status (38)
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| JP (2) | JP6006308B2 (es) |
| KR (1) | KR101946664B1 (es) |
| CN (1) | CN103781781B (es) |
| AR (2) | AR087168A1 (es) |
| AU (2) | AU2012282316B2 (es) |
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| EC (1) | ECSP14013130A (es) |
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Families Citing this family (10)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JP2013531027A (ja) | 2010-07-13 | 2013-08-01 | アストラゼネカ・アクチエボラーグ | N−[2−[[(2,3−ジフルオロフェニル)メチル]チオ]−6−{[(1r,2s)−2,3−ジヒドロキシ−1−メチルプロピル]オキシ}−4−ピリミジニル]−1−アゼチジンスルホンアミドの新規結晶形態 |
| LT3255043T (lt) * | 2011-07-12 | 2021-04-12 | Astrazeneca Ab | N-(6-((2r,3s)-3,4-dihidroksibutan-2-iloksi)-2-(4-fluorbenziltio)pirimidin-4-il)-3- metilazetidin-1-sulfonamidas kaip chemokino receptoriaus moduliatorius |
| EP2740458B1 (en) * | 2012-12-06 | 2016-08-03 | IP Gesellschaft für Management mbH | Packaging comprising forms of sodium salt of 4-tert-butyl-N-[4-chloro-2-(1-oxy-pyridine-4-carbonyl)-phenyl]-benzenesulfonamide |
| US10772886B2 (en) * | 2016-03-11 | 2020-09-15 | Ardea Biosciences, Inc. | CXCR-2 inhibitors for treating crystal arthropathy disorders |
| CN111356675A (zh) * | 2017-09-12 | 2020-06-30 | 阿迪亚生命科学公司 | 用于治疗病症的cxcr-2抑制剂 |
| HUE063987T2 (hu) * | 2019-06-12 | 2024-02-28 | Nouryon Chemicals Int Bv | Eljárás karbonsav izolálására vizes mellékáramból |
| EP3983380B1 (en) | 2019-06-12 | 2023-08-02 | Nouryon Chemicals International B.V. | Process for the production of peroxyesters |
| EP3983369B1 (en) | 2019-06-12 | 2023-08-02 | Nouryon Chemicals International B.V. | Process for the production of diacyl peroxides |
| WO2020249691A1 (en) | 2019-06-12 | 2020-12-17 | Nouryon Chemicals International B.V. | Process for the production of diacyl peroxides |
| HUE063679T2 (hu) | 2019-06-12 | 2024-01-28 | Nouryon Chemicals Int Bv | Eljárás diacil-peroxidok elõállítására |
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| US3457278A (en) * | 1964-10-15 | 1969-07-22 | Geigy Chem Corp | Cyclopropyl-4-sulfanilamido-pyrimidines |
| GB9624482D0 (en) | 1995-12-18 | 1997-01-15 | Zeneca Phaema S A | Chemical compounds |
| ATE237596T1 (de) | 1996-02-13 | 2003-05-15 | Astrazeneca Ab | Chinazolinderivate und deren verwendung als vegf hemmer |
| US6291455B1 (en) | 1996-03-05 | 2001-09-18 | Zeneca Limited | 4-anilinoquinazoline derivatives |
| GB9718972D0 (en) | 1996-09-25 | 1997-11-12 | Zeneca Ltd | Chemical compounds |
| GB9714249D0 (en) | 1997-07-08 | 1997-09-10 | Angiogene Pharm Ltd | Vascular damaging agents |
| FI981521A0 (fi) * | 1998-07-01 | 1998-07-01 | Orion Corp | Substituoidut beta-diketonit ja niiden käyttö |
| GB9900334D0 (en) | 1999-01-07 | 1999-02-24 | Angiogene Pharm Ltd | Tricylic vascular damaging agents |
| GB9900752D0 (en) | 1999-01-15 | 1999-03-03 | Angiogene Pharm Ltd | Benzimidazole vascular damaging agents |
| NZ522074A (en) | 2000-05-31 | 2004-06-25 | Astrazeneca Ab | Indole derivatives with vascular damaging activity |
| NZ522661A (en) | 2000-07-07 | 2004-07-30 | Angiogene Pharm Ltd | Colchinol derivatives as angiogenesis inhibitors |
| CA2411160A1 (en) | 2000-07-07 | 2002-01-17 | Angiogene Pharmaceuticals Limited | Colchinol derivatives as vascular damaging agents |
| GB0217431D0 (en) | 2002-07-27 | 2002-09-04 | Astrazeneca Ab | Novel compounds |
| GB0419235D0 (en) * | 2004-08-28 | 2004-09-29 | Astrazeneca Ab | Compounds |
| ME01620B (me) * | 2004-08-28 | 2014-09-20 | Astrazeneca Ab | Pirimidin sulfonamidni derivati kao modulatori hemokinskih receptora |
| BRPI0621226A2 (pt) * | 2006-01-19 | 2012-07-10 | Orchid Reseach Lab Ltd | compostos heterociclos |
| WO2008157273A1 (en) * | 2007-06-14 | 2008-12-24 | Smithkline Beecham Corporation | Chemical compounds |
| TW201006824A (en) * | 2008-07-16 | 2010-02-16 | Astrazeneca Ab | Novel compound 395 |
| JP2011529027A (ja) | 2008-07-25 | 2011-12-01 | ビーエーエスエフ ソシエタス・ヨーロピア | 3−アミノメチル−1−シクロヘキシルアミン、及びその製造方法 |
| JP2013531027A (ja) * | 2010-07-13 | 2013-08-01 | アストラゼネカ・アクチエボラーグ | N−[2−[[(2,3−ジフルオロフェニル)メチル]チオ]−6−{[(1r,2s)−2,3−ジヒドロキシ−1−メチルプロピル]オキシ}−4−ピリミジニル]−1−アゼチジンスルホンアミドの新規結晶形態 |
| LT3255043T (lt) * | 2011-07-12 | 2021-04-12 | Astrazeneca Ab | N-(6-((2r,3s)-3,4-dihidroksibutan-2-iloksi)-2-(4-fluorbenziltio)pirimidin-4-il)-3- metilazetidin-1-sulfonamidas kaip chemokino receptoriaus moduliatorius |
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2012
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