WO2009001374A3 - Preparation of ethyl-3'-[((7-chloro-2-quinolinyl)ethenyl)phenyl]-3-oxopropanoate, a key intermediate for montelukast sodium - Google Patents
Preparation of ethyl-3'-[((7-chloro-2-quinolinyl)ethenyl)phenyl]-3-oxopropanoate, a key intermediate for montelukast sodium Download PDFInfo
- Publication number
- WO2009001374A3 WO2009001374A3 PCT/IN2008/000398 IN2008000398W WO2009001374A3 WO 2009001374 A3 WO2009001374 A3 WO 2009001374A3 IN 2008000398 W IN2008000398 W IN 2008000398W WO 2009001374 A3 WO2009001374 A3 WO 2009001374A3
- Authority
- WO
- WIPO (PCT)
- Prior art keywords
- ethenyl
- quinolinyl
- chloro
- ethyl
- phenyl
- Prior art date
Links
- -1 (7-chloro-2-quinolinyl)ethenyl Chemical group 0.000 title abstract 7
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 title abstract 3
- 229960001951 montelukast sodium Drugs 0.000 title 1
- LBFBRXGCXUHRJY-HKHDRNBDSA-M montelukast sodium Chemical compound [Na+].CC(C)(O)C1=CC=CC=C1CC[C@H](C=1C=C(\C=C\C=2N=C3C=C(Cl)C=CC3=CC=2)C=CC=1)SCC1(CC([O-])=O)CC1 LBFBRXGCXUHRJY-HKHDRNBDSA-M 0.000 title 1
- ZMIZHFVHQFYHTJ-UHFFFAOYSA-N 3-[2-(7-chloroquinolin-2-yl)ethenyl]-2-ethylbenzaldehyde Chemical compound CCC1=C(C=O)C=CC=C1C=CC1=CC=C(C=CC(Cl)=C2)C2=N1 ZMIZHFVHQFYHTJ-UHFFFAOYSA-N 0.000 abstract 2
- WQZQFYRSYLXBGP-UHFFFAOYSA-N 7-chloro-2-methylquinoline Chemical compound C1=CC(Cl)=CC2=NC(C)=CC=C21 WQZQFYRSYLXBGP-UHFFFAOYSA-N 0.000 abstract 2
- 125000000217 alkyl group Chemical group 0.000 abstract 2
- WPYMKLBDIGXBTP-UHFFFAOYSA-N benzoic acid Chemical compound OC(=O)C1=CC=CC=C1 WPYMKLBDIGXBTP-UHFFFAOYSA-N 0.000 abstract 2
- 150000001875 compounds Chemical class 0.000 abstract 2
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 abstract 2
- 239000002184 metal Substances 0.000 abstract 2
- 239000012027 Collins reagent Substances 0.000 abstract 1
- 150000004703 alkoxides Chemical class 0.000 abstract 1
- 125000005907 alkyl ester group Chemical group 0.000 abstract 1
- IZALUMVGBVKPJD-UHFFFAOYSA-N benzene-1,3-dicarbaldehyde Chemical compound O=CC1=CC=CC(C=O)=C1 IZALUMVGBVKPJD-UHFFFAOYSA-N 0.000 abstract 1
- 239000003054 catalyst Substances 0.000 abstract 1
- 238000004519 manufacturing process Methods 0.000 abstract 1
- 229910052987 metal hydride Inorganic materials 0.000 abstract 1
- 150000004681 metal hydrides Chemical class 0.000 abstract 1
- 239000003960 organic solvent Substances 0.000 abstract 1
- NPRDHMWYZHSAHR-UHFFFAOYSA-N pyridine;trioxochromium Chemical compound O=[Cr](=O)=O.C1=CC=NC=C1.C1=CC=NC=C1 NPRDHMWYZHSAHR-UHFFFAOYSA-N 0.000 abstract 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D215/00—Heterocyclic compounds containing quinoline or hydrogenated quinoline ring systems
- C07D215/02—Heterocyclic compounds containing quinoline or hydrogenated quinoline ring systems having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen atoms or carbon atoms directly attached to the ring nitrogen atom
- C07D215/16—Heterocyclic compounds containing quinoline or hydrogenated quinoline ring systems having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen atoms or carbon atoms directly attached to the ring nitrogen atom with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached to ring carbon atoms
- C07D215/18—Halogen atoms or nitro radicals
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Quinoline Compounds (AREA)
Abstract
A process for preparing β- ketoester of formula (III) comprises; (a)condensing alkyl 3- formylbenzoate with 7-Chloroquinaldine to give alkyl 3-[((7-chloro-2-quinolinyl) ethenyl)] benzoate; and (b) reacting alkyl 3-[((7-chloro-2-quinolinyl) ethenyl)] benzoate with an alkyl ester in presence of metal hydride/metal alkoxides to obtain a compound β- ketoester of structural formula (Ill) or (a) condensing isophthalaldehyde with 7-Chloroquinaldine to give Ethyl 3-[((7-chloro-2- quinolinyl) ethenyl)] benzaldehyde (b) reacting Ethyl 3-[((7-chloro-2-quinolinyl) ethenyl)] benzaldehyde with an α-halo ester in presence of a metal catalyst to give Ethyl 3'-[((7-chloro- 2-quinolinyl) ethenyl)phenyl] -3 -hydroxy propanoate; and (c) treating Ethyl 3'-[((7-chloro-2- quinolinyl)ethenyl)phenyl]-3-hydroxy propanoate with Collins reagent in an organic solvent to obtain a compound β- ketoester of structural formula (III).
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| IN1353CH2007 | 2007-06-25 | ||
| IN1353/CHE/2007 | 2007-06-25 |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| WO2009001374A2 WO2009001374A2 (en) | 2008-12-31 |
| WO2009001374A3 true WO2009001374A3 (en) | 2011-06-30 |
Family
ID=40186130
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| PCT/IN2008/000398 WO2009001374A2 (en) | 2007-06-25 | 2008-06-24 | Preparation of ethyl-3'-[((7-chloro-2-quinolinyl)ethenyl)phenyl]-3-oxopropanoate, a key intermediate for montelukast sodium |
Country Status (1)
| Country | Link |
|---|---|
| WO (1) | WO2009001374A2 (en) |
Families Citing this family (5)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| WO2008035379A2 (en) * | 2006-09-19 | 2008-03-27 | Aptuit Laurus Private Limited | Process for and intermediates of leukotriene antagonists |
| HUP1000425A2 (en) | 2010-08-11 | 2012-03-28 | Richter Gedeon Nyrt | Process for the production of montelukast sodium |
| WO2014081616A1 (en) * | 2012-11-21 | 2014-05-30 | Merck Sharp & Dohme Corp. | Preparation of precursors for leukotriene antagonists |
| CN104109122B (en) * | 2013-04-16 | 2017-03-29 | 浙江奥翔药业股份有限公司 | For synthesizing midbody compound of montelukast and preparation method thereof |
| CN116375639B (en) * | 2023-04-19 | 2024-05-28 | 南京欧信医药技术有限公司 | Method for preparing montelukast sodium intermediate by micro-channel method |
Citations (4)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| EP0375348A1 (en) * | 1988-12-23 | 1990-06-27 | Smithkline Beecham Corporation | Leukotriene antagonists |
| EP0480716A1 (en) * | 1990-10-12 | 1992-04-15 | Merck Frosst Canada Inc. | Saturated hydroxyalkylquinoline acids as leukotriene antagonists |
| US5869673A (en) * | 1997-02-28 | 1999-02-09 | Merck & Co., Inc. | Process for 3-(2-(7-chloro-2-quinolinyl)ethenyl) - benzaldehyde |
| US20030195201A1 (en) * | 2001-12-10 | 2003-10-16 | Bo Yunxin Y. | Vanilloid receptor ligands and their use in treatments |
-
2008
- 2008-06-24 WO PCT/IN2008/000398 patent/WO2009001374A2/en active Application Filing
Patent Citations (4)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| EP0375348A1 (en) * | 1988-12-23 | 1990-06-27 | Smithkline Beecham Corporation | Leukotriene antagonists |
| EP0480716A1 (en) * | 1990-10-12 | 1992-04-15 | Merck Frosst Canada Inc. | Saturated hydroxyalkylquinoline acids as leukotriene antagonists |
| US5869673A (en) * | 1997-02-28 | 1999-02-09 | Merck & Co., Inc. | Process for 3-(2-(7-chloro-2-quinolinyl)ethenyl) - benzaldehyde |
| US20030195201A1 (en) * | 2001-12-10 | 2003-10-16 | Bo Yunxin Y. | Vanilloid receptor ligands and their use in treatments |
Non-Patent Citations (1)
| Title |
|---|
| OKARNOTO ET AL.: "A Novel Dual Antagonist of Thromboxane A2 and Leukotriene D4 Receptors: Synthesis and Structure-Activity Relationships of Chioroquinolylvinyl Derivatives", CHEMICAL & PHARMACEUTICAL BULLETIN, vol. 54, no. 5, 2006, pages 603 - 610 * |
Also Published As
| Publication number | Publication date |
|---|---|
| WO2009001374A2 (en) | 2008-12-31 |
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