WO2013121439A3 - Garenoxacin mesylate, process for preparation thereof, and crystalline form thereof. - Google Patents
Garenoxacin mesylate, process for preparation thereof, and crystalline form thereof. Download PDFInfo
- Publication number
- WO2013121439A3 WO2013121439A3 PCT/IN2013/000090 IN2013000090W WO2013121439A3 WO 2013121439 A3 WO2013121439 A3 WO 2013121439A3 IN 2013000090 W IN2013000090 W IN 2013000090W WO 2013121439 A3 WO2013121439 A3 WO 2013121439A3
- Authority
- WO
- WIPO (PCT)
- Prior art keywords
- garenoxacin
- mesylate
- crystalline form
- preparation
- peaks
- Prior art date
Links
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D401/00—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom
- C07D401/02—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing two hetero rings
- C07D401/04—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing two hetero rings directly linked by a ring-member-to-ring-member bond
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- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
Abstract
Provided are garenoxacin mesylate, process for preparation thereof, and crystalline form thereof. The garenoxacin mesylate crystalline form is characterized by an X-ray powder diffraction pattern with peaks at about 13.77, 20.54, 21.50, 21.77, 22.12 and 23.90±0.20. A pharmaceutical composition of the garenoxacin mesylate crystalline form is also provided.
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
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IN419/MUM/2012 | 2012-02-15 | ||
IN419MU2012 | 2012-02-15 |
Publications (2)
Publication Number | Publication Date |
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WO2013121439A2 WO2013121439A2 (en) | 2013-08-22 |
WO2013121439A3 true WO2013121439A3 (en) | 2013-10-24 |
Family
ID=48984863
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
PCT/IN2013/000090 WO2013121439A2 (en) | 2012-02-15 | 2013-02-11 | Process for garenoxacin mesylate |
Country Status (1)
Country | Link |
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WO (1) | WO2013121439A2 (en) |
Families Citing this family (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN105801482B (en) * | 2016-04-18 | 2018-06-22 | 浙江中欣氟材股份有限公司 | A kind of preparation method of the bromo- 8- difluoro-methoxies -1,4- dihydroquinoline -3- carboxylic acid, ethyl esters of 1- cyclopropyl -4- oxos -7- |
CN105777631B (en) * | 2016-04-18 | 2018-06-29 | 浙江中欣氟材股份有限公司 | A kind of synthetic method of the bromo- 8- difluoro-methoxies -1,4- dihydroquinoline -3- carboxylic acid, ethyl esters of 1- cyclopropyl -4- oxos -7- |
CN105801390A (en) * | 2016-04-18 | 2016-07-27 | 浙江中欣氟材股份有限公司 | Method for synthesizing 2,4-dibromo-3-difluoromethoxy acetophenone |
Citations (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US6025370A (en) * | 1996-02-09 | 2000-02-15 | Toyama Chemical Co., Ltd. | Quinolonecarboxylic acid derivatives or salts thereof |
JP2000229946A (en) * | 1998-12-10 | 2000-08-22 | Toyama Chem Co Ltd | Production of quinolonecarboxylic acid and its intermediate |
US6337399B1 (en) * | 1997-10-27 | 2002-01-08 | Toyama Chemical Co., Ltd. | Processes for producing 7-isoindolinequinolonecarboxylic derivatives and intermediates therefor, salts of 7-isoindolinequinolonecarboxylic acids, hydrates thereof, and composition containing the same as active ingredient |
JP2003206290A (en) * | 2001-11-06 | 2003-07-22 | Toyama Chem Co Ltd | Non-solvate of 2-[(1r)-1-methyl-2-trityl-2,3-dihydro-1h-5 isoindolyl]-1,3,6,2-dioxaazaborocane and method for producing the same |
-
2013
- 2013-02-11 WO PCT/IN2013/000090 patent/WO2013121439A2/en active Application Filing
Patent Citations (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US6025370A (en) * | 1996-02-09 | 2000-02-15 | Toyama Chemical Co., Ltd. | Quinolonecarboxylic acid derivatives or salts thereof |
US6337399B1 (en) * | 1997-10-27 | 2002-01-08 | Toyama Chemical Co., Ltd. | Processes for producing 7-isoindolinequinolonecarboxylic derivatives and intermediates therefor, salts of 7-isoindolinequinolonecarboxylic acids, hydrates thereof, and composition containing the same as active ingredient |
JP2000229946A (en) * | 1998-12-10 | 2000-08-22 | Toyama Chem Co Ltd | Production of quinolonecarboxylic acid and its intermediate |
JP2003206290A (en) * | 2001-11-06 | 2003-07-22 | Toyama Chem Co Ltd | Non-solvate of 2-[(1r)-1-methyl-2-trityl-2,3-dihydro-1h-5 isoindolyl]-1,3,6,2-dioxaazaborocane and method for producing the same |
Non-Patent Citations (5)
Title |
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DANESHTALAB, MOHSEN: "Novel synthetic antibacterial agents", TOPICS IN HETEROCYCLIC CHEMISTRY, vol. 2, 2006, pages 153 - 206 * |
GRAUL, A. ET AL.: "T-3811ME: quinolone antibacterial", DRUGS OF THE FUTURE, vol. 12, no. 24, 1999, pages 1324 - 1331 * |
HAYASHI, KAZUYA ET AL.: "Synthesis, antibacterial activity, and toxicity of 7-(isoindolin-5-yl)-4-oxoquinoline-3-carboxylic acids: Discovery of the novel Des-F (6)-quinolone antibacterial agent garenoxacin (T-3811 or BMS-284756)", ARZNEIMITTEL-FORSCHUNG, vol. 12, no. 52, 2002, pages 903 - 913 * |
WANG, XIUYUN ET AL.: "Synthesis and antibacterial activities of Garenoxacin", WORLD NOTES ON ANTIBIOTICS, vol. 3, no. 27, 2006, pages 100 - 104 * |
WU, XIAOGUO ET AL.: "The synthesis of Garenoxacin", CHINESE JOURNAL OF MODEM APPLIED PHARMACY, vol. 3, no. 26, 2009, pages 218 - 220 * |
Also Published As
Publication number | Publication date |
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WO2013121439A2 (en) | 2013-08-22 |
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