KR970042550A - Cdch의 신규 결정성 변형체, 그의 제조 방법 및 이 변형체를 함유하는 제약 제제 - Google Patents
Cdch의 신규 결정성 변형체, 그의 제조 방법 및 이 변형체를 함유하는 제약 제제 Download PDFInfo
- Publication number
- KR970042550A KR970042550A KR1019960064345A KR19960064345A KR970042550A KR 970042550 A KR970042550 A KR 970042550A KR 1019960064345 A KR1019960064345 A KR 1019960064345A KR 19960064345 A KR19960064345 A KR 19960064345A KR 970042550 A KR970042550 A KR 970042550A
- Authority
- KR
- South Korea
- Prior art keywords
- cdch
- monohydrate
- variants
- compound according
- anhydrous
- Prior art date
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Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D471/00—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, at least one ring being a six-membered ring with one nitrogen atom, not provided for by groups C07D451/00 - C07D463/00
- C07D471/02—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, at least one ring being a six-membered ring with one nitrogen atom, not provided for by groups C07D451/00 - C07D463/00 in which the condensed system contains two hetero rings
- C07D471/04—Ortho-condensed systems
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P31/00—Antiinfectives, i.e. antibiotics, antiseptics, chemotherapeutics
- A61P31/04—Antibacterial agents
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- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Health & Medical Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- General Health & Medical Sciences (AREA)
- General Chemical & Material Sciences (AREA)
- Medicinal Chemistry (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Oncology (AREA)
- Pharmacology & Pharmacy (AREA)
- Communicable Diseases (AREA)
- Animal Behavior & Ethology (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Public Health (AREA)
- Veterinary Medicine (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Nitrogen Condensed Heterocyclic Rings (AREA)
- Plural Heterocyclic Compounds (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Acyclic And Carbocyclic Compounds In Medicinal Compositions (AREA)
Abstract
본 발명은 1-시클로프로필-7-([S,S]-2,8-디아자비시클로-[4,3,0]논-8-일)-6-플루오로-1,4-디히드로-8-메톡시-4-옥소-3-퀴놀린카르복실산 히드로클로라이드 (CDCH)의 신규 일수화물, 그의 제조 방법 및 활성 화합물로서 일수화물을 함유하는 제약 제제에 관한 것이다.
Description
본 내용은 요부공개 건이므로 전문내용을 수록하지 않았음
내용없음
Claims (10)
13C-NMR 스펙트럼에서는 168.1 ppm에서 특성 피크를 가지고 X선 회절도 에서는 2Θ=26.7에서 띠를 가진 하기 화학식 1의 CDCH 일수화물
제1항에 있어서, 사방결정형인 화합물.
무수 CDCH를 화학양론적 양의 결정화수가 흡수되고 결정의 변환이 종결될 때까지 완전히 혼합 및 수화하기에 충분한 양 이상의 물로 처리한 후에, 이와 같이 하여 얻어진 일수화물의 결정을 분리하고, 남아있는 흡수된 물을 제거하는 것이 특징인 제1항에 따른 CDCH 일수화물의 제조방법.
제3항에 있어서, 수성 매질 중의 무수 CDCH의 현탁액을 수화 및 결정 변환이 종결될 때까지 교반하는 것이 특징인 방법.
제3항에 있어서, 사방결정형 일수화물을 제조하기 위해서는, 화학양론적으로 충분하되 10% 이하의 물 함량을 가진 매질 중에 침상 무수 CDCH 또는 CDCH 일수화물을 용해시킨 다음, 용매를 제거하는 것이 특징인 방법.
제3항에 있어서, 무수 CDCH가 결정이 정량적으로 변환될 때까지 습기에 노출시키는 것이 특징인 방법.
제1항 또는 제2항에 따른 화합물을 함유하는 약제.
제1항 또는 제2항에 따른 화합물을 함유하는 항균 제제.
제1항 또는 제2항에 따른 화합물의 용도.
제1항 또는 제2항에 따른 화합물의 약제 제조 용도.
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
DE19546249A DE19546249A1 (de) | 1995-12-12 | 1995-12-12 | Neue Kristallmodifikation des 1-Cyclopropyl-7-([S,S]-2,8-diazabicyclo[4,3,0]non-8-yl)-6-fluor-1,4-dihydro-8-methoxy-4-oxo-3-chinolincarbonsäure Hydrochlorid (CDCH), Verfahren zu dessen Herstellung und diese enthaltende pharmazeutische Zubereitungen |
DE19546249.1 | 1995-12-12 |
Publications (2)
Publication Number | Publication Date |
---|---|
KR970042550A true KR970042550A (ko) | 1997-07-24 |
KR100525146B1 KR100525146B1 (ko) | 2006-01-27 |
Family
ID=7779831
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
KR1019960064345A KR100525146B1 (ko) | 1995-12-12 | 1996-12-11 | Cdch의신규결정성변형체,그의제조방법및이변형체를함유하는 항균 조성물 |
Country Status (42)
Country | Link |
---|---|
US (1) | US5849752A (ko) |
EP (1) | EP0780390B1 (ko) |
JP (1) | JP4104687B2 (ko) |
KR (1) | KR100525146B1 (ko) |
CN (1) | CN1061348C (ko) |
AR (1) | AR005009A1 (ko) |
AT (1) | ATE221531T1 (ko) |
AU (1) | AU708006B2 (ko) |
BG (1) | BG62258B1 (ko) |
BR (1) | BR9605968A (ko) |
CA (1) | CA2192418C (ko) |
CO (1) | CO4480105A1 (ko) |
CU (1) | CU22774A3 (ko) |
CZ (1) | CZ288657B6 (ko) |
DE (2) | DE19546249A1 (ko) |
DK (1) | DK0780390T3 (ko) |
EE (1) | EE03474B1 (ko) |
ES (1) | ES2179910T3 (ko) |
HR (1) | HRP960558B1 (ko) |
HU (1) | HU226521B1 (ko) |
ID (1) | ID22625A (ko) |
IL (1) | IL119795A (ko) |
IN (1) | IN185805B (ko) |
MA (1) | MA24342A1 (ko) |
MY (1) | MY117492A (ko) |
NL (1) | NL300109I1 (ko) |
NO (1) | NO306725B1 (ko) |
NZ (1) | NZ299905A (ko) |
PL (1) | PL184885B1 (ko) |
PT (1) | PT780390E (ko) |
RO (1) | RO119782B1 (ko) |
RU (1) | RU2162468C2 (ko) |
SA (1) | SA96170492B1 (ko) |
SG (1) | SG47201A1 (ko) |
SI (1) | SI0780390T1 (ko) |
SK (1) | SK282805B6 (ko) |
SV (1) | SV1996000109A (ko) |
TR (1) | TR199600970A2 (ko) |
TW (1) | TW411340B (ko) |
UA (1) | UA35638C2 (ko) |
YU (1) | YU49485B (ko) |
ZA (1) | ZA9610405B (ko) |
Families Citing this family (36)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
PL192273B1 (pl) * | 1997-09-25 | 2006-09-29 | Bayer Ag | Preparat środka leczniczego w postaci pastylki o kontrolowanej dyfuzji lub w postaci układu matrycowego, o kontrolowanym uwalnianiu substancji czynnej |
DE19751948A1 (de) * | 1997-11-24 | 1999-05-27 | Bayer Ag | Verfahren zur Herstellung von 8-Methoxy-Chinoloncarbonsäuren |
US6509327B1 (en) | 1998-09-30 | 2003-01-21 | Alcon Manufacturing, Ltd. | Compositions and methods for treating otic, ophthalmic and nasal infections |
US6716830B2 (en) | 1998-09-30 | 2004-04-06 | Alcon, Inc. | Ophthalmic antibiotic compositions containing moxifloxacin |
US6395746B1 (en) | 1998-09-30 | 2002-05-28 | Alcon Manufacturing, Ltd. | Methods of treating ophthalmic, otic and nasal infections and attendant inflammation |
HU229065B1 (en) | 1998-11-10 | 2013-07-29 | Bayer Ip Gmbh | Pharmaceutical moxifloxacin compositions |
DE19854357A1 (de) * | 1998-11-25 | 2000-05-31 | Bayer Ag | Semi-Hydrochlorid von 8-Cyan-1-cyclopropyl-7-(1S,6S-2,8-diazabicyclo/4.3.0/ -nonan-8-yl)-6-fluor-1,4-dihydro-4-oxo-3-chinolincarbonsäure |
DE19854355A1 (de) * | 1998-11-25 | 2000-05-31 | Bayer Ag | Kristallmodifikation B von 8-Cyan-1-cyclopropyl-7-(1S, 6S-2,8-diazabicyclo-/4.3.O/nonan-8-yl)-6-fluor-1,4-dihydro-4-oxo-3-chinolincarbonsäure |
DE19854356A1 (de) * | 1998-11-25 | 2000-05-31 | Bayer Ag | Kristallmodifikation A von 8-Cyan-1-cyclopropyl-7-(1S,6S-2,8-diazabicyclo-/4.3.0/nonan-8-yl)-6-fluor-1,4-dihydro-4-oxo-3-chinolincarbonsäure |
DE19908449A1 (de) * | 1999-02-26 | 2000-08-31 | Bayer Ag | Kristallmodifikation C von 8-Cyan-1-cyclopropyl-7-(1S,6S-2,8-diazabicylo-[4.3.0]nonan-8-yl)-6-fluor-1,4-dihydro-4-oxo-3-chino/incarbonsäure |
EP1562942A1 (en) * | 2002-10-31 | 2005-08-17 | Ranbaxy Laboratories, Ltd. | Amorphous moxifloxacin hydrochloride |
US7230006B2 (en) * | 2003-04-09 | 2007-06-12 | Reddy's Laboratories Limited | Crystalline form III of anhydrous moxifloxacin hydrochloride and a process for preparation thereof |
US20060264635A1 (en) * | 2003-08-05 | 2006-11-23 | Chava Satyanarayana | Process for the preparation of moxifloxacin hydrochloride |
ITMI20032259A1 (it) | 2003-11-20 | 2005-05-21 | Chemi Spa | Nuovo polimorfo dell'acido 1-ciclopropil-7-(s,s-2,8-diazabciclo-4.3.0-non-8-il)-6-fluoro-1,4-diidro-8-metossi-4-oxo-chinolin carbossilico cloridrato e metodi per la sua preparazione |
ES2319125T3 (es) * | 2003-11-20 | 2009-05-04 | Chemi S.P.A. | Polimorfos del clorhidrato del acido 1-ciclopropil-7-((s,s)-2,8-diazadiciclo(4.3.0)-non-8-il)-6-fluoro-1,4-dihidro-8-metoxi-4-oxo-3-quinolina carboxilico y metodos para la preparacion de los mismos. |
US7491725B2 (en) | 2004-02-06 | 2009-02-17 | Bristol-Myers Squibb Company | Process for preparing 2-aminothiazole-5-aromatic carboxamides as kinase inhibitors |
DE102004063347A1 (de) * | 2004-12-23 | 2006-07-13 | Stada Arzneimittel Ag | Gebrauchsfertige Gemcitabinlösungen und Gemcitabinlösungskonzentrate |
WO2007033515A1 (fr) * | 2005-09-21 | 2007-03-29 | Shenzhen Tys R & D Co., Ltd. | Formulation orale contenant de la moxifloxacine et son procédé de préparation |
GB0612422D0 (en) * | 2006-06-23 | 2006-08-02 | Generics Uk Ltd | Novel hydrate form |
EP2032521B1 (en) | 2006-06-27 | 2009-10-28 | Sandoz AG | New method for salt preparation |
ES2303768B1 (es) * | 2006-09-08 | 2009-06-05 | Quimica Sintetica, S.A. | Nueva forma cristalina de moxifloxacino clorhidrato. |
AU2007320997B2 (en) | 2006-11-13 | 2012-11-08 | Cipla Limited | Process for the synthesis of moxifloxacin hydrochloride |
EP1992626A1 (en) * | 2007-05-10 | 2008-11-19 | Sandoz AG | Process for the preparation of moxifloxacin hydrochloride |
EP2083010A1 (en) * | 2008-01-08 | 2009-07-29 | Chemo Ibérica, S.A. | Polymorphic Forms of Moxifloxacin hydrochloride and processes for preparation thereof |
EP2154137A1 (en) | 2008-08-04 | 2010-02-17 | Chemo Ibérica, S.A. | Crystalline form of moxifloxacin base |
CN102176902B (zh) * | 2008-10-09 | 2012-10-31 | 阿卜迪易卜拉欣贸易公司 | 有机溶剂在莫西沙星湿法造粒中的应用 |
EP2342204A1 (en) * | 2008-11-06 | 2011-07-13 | Hetero Research Foundation | Novel polymorph of moxifloxacin hydrochloride |
WO2010066385A1 (de) | 2008-12-08 | 2010-06-17 | Ratiopharm Gmbh | Kompaktiertes moxifloxacin |
EP2429991B1 (en) | 2009-05-15 | 2014-09-10 | Redx Pharma Limited | Redox drug derivatives |
WO2011121596A2 (en) * | 2010-04-01 | 2011-10-06 | Neuland Laboratories Ltd. | Crystal modification of moxifloxacin hydrochloride |
BRPI1106900A2 (pt) | 2011-12-26 | 2013-11-05 | Ems Sa | Composição farmacêutica sólida compreendendo antibótico da familia das quinolonas e processo de sua obtenção |
FR2992218B1 (fr) | 2012-06-22 | 2015-01-23 | Rivopharm Sa | Composition pharmaceutique de chlorhydrate de moxifloxacine et procede de preparation |
CN102924449B (zh) * | 2012-10-30 | 2015-08-12 | 重庆福安药业集团庆余堂制药有限公司 | 盐酸莫西沙星h晶型及其制备方法和药物组合物 |
US9388178B2 (en) | 2012-12-04 | 2016-07-12 | Mankind Research Centre | Process for the preparation of moxifloxacin hydrochloride |
RU2561037C2 (ru) * | 2013-02-07 | 2015-08-20 | Открытое акционерное общество "Химико-фармацевтический комбинат "АКРИХИН" (ОАО "АКРИХИН") | Антибактериальная фармацевтическая композиция и способ ее получения |
EP2969004A4 (en) | 2013-03-15 | 2016-09-21 | Melinta Therapeutics Inc | METHOD FOR THE TREATMENT OF INFECTIONS IN OVERWEIGHT AND ADIPOSIVE PATIENTS USING ANTIBIOTICS |
Family Cites Families (10)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
DE3601567A1 (de) * | 1986-01-21 | 1987-07-23 | Bayer Ag | 7-(azabicycloalkyl)-chinoloncarbonsaeure- und -naphthyridon-carbonsaeure-derivate |
CN1019114B (zh) * | 1986-03-31 | 1992-11-18 | 三共株式会社 | 喹啉-3-羟酸衍生物的制备方法 |
AU609974B2 (en) * | 1988-05-18 | 1991-05-09 | Warner-Lambert Company | Improved process for the preparation of 5-amino-7- (substituted amino)-quinoline-3-carboxylic acids |
DE3910663A1 (de) * | 1989-04-03 | 1990-10-04 | Bayer Ag | 5-alkylchinoloncarbonsaeuren |
TW209865B (ko) | 1992-01-10 | 1993-07-21 | Bayer Ag | |
DE69331003T2 (de) * | 1992-01-31 | 2002-06-20 | Chugai Seiyaku K.K., Tokio/Tokyo | Kristalle von derivaten von chinozon carbonsäure-hydraten |
DE4234078A1 (de) | 1992-10-09 | 1994-04-14 | Bayer Ag | Chinoloncarbonsäuren |
NO301165B1 (no) * | 1992-12-25 | 1997-09-22 | Daiichi Seiyaku Co | Bicykliske aminderivater og antibakterielle midler inneholdende disse |
ZA946853B (en) * | 1993-09-10 | 1995-04-24 | Daiichi Seiyaku Co | Crystals of antimicrobial compound. |
DE69504392T2 (de) * | 1994-04-07 | 1999-02-11 | Pfizer Inc., New York, N.Y. | Verwendung von Trovafloxacin oder dessen Derivaten zur Herstellung eines Arzneimittels zur Behandlung von H.Pylori Infektionen |
-
1995
- 1995-12-12 DE DE19546249A patent/DE19546249A1/de not_active Withdrawn
-
1996
- 1996-11-22 MA MA24398A patent/MA24342A1/fr unknown
- 1996-11-25 HR HR960558A patent/HRP960558B1/xx not_active IP Right Cessation
- 1996-11-25 RO RO96-02223A patent/RO119782B1/ro unknown
- 1996-11-27 CU CU1996111A patent/CU22774A3/es not_active IP Right Cessation
- 1996-11-29 DE DE59609501T patent/DE59609501D1/de not_active Expired - Lifetime
- 1996-11-29 ES ES96119134T patent/ES2179910T3/es not_active Expired - Lifetime
- 1996-11-29 EP EP96119134A patent/EP0780390B1/de not_active Expired - Lifetime
- 1996-11-29 PT PT96119134T patent/PT780390E/pt unknown
- 1996-11-29 SI SI9630468T patent/SI0780390T1/xx unknown
- 1996-11-29 DK DK96119134T patent/DK0780390T3/da active
- 1996-11-29 AT AT96119134T patent/ATE221531T1/de active
- 1996-12-05 US US08/760,543 patent/US5849752A/en not_active Expired - Lifetime
- 1996-12-05 TR TR96/00970A patent/TR199600970A2/xx unknown
- 1996-12-06 YU YU65096A patent/YU49485B/sh unknown
- 1996-12-06 IN IN2723DE1996 patent/IN185805B/en unknown
- 1996-12-06 TW TW085115048A patent/TW411340B/zh not_active IP Right Cessation
- 1996-12-06 AU AU74216/96A patent/AU708006B2/en not_active Expired
- 1996-12-09 AR ARP960105569A patent/AR005009A1/es active IP Right Grant
- 1996-12-09 NZ NZ299905A patent/NZ299905A/en not_active IP Right Cessation
- 1996-12-09 CA CA002192418A patent/CA2192418C/en not_active Expired - Lifetime
- 1996-12-10 SG SG1996011612A patent/SG47201A1/en unknown
- 1996-12-10 JP JP34450296A patent/JP4104687B2/ja not_active Expired - Lifetime
- 1996-12-10 IL IL11979596A patent/IL119795A/en not_active IP Right Cessation
- 1996-12-10 CO CO96064770A patent/CO4480105A1/es unknown
- 1996-12-10 PL PL96317415A patent/PL184885B1/pl unknown
- 1996-12-10 BG BG101043A patent/BG62258B1/bg unknown
- 1996-12-10 ID IDP963684A patent/ID22625A/id unknown
- 1996-12-11 ZA ZA9610405A patent/ZA9610405B/xx unknown
- 1996-12-11 MY MYPI96005214A patent/MY117492A/en unknown
- 1996-12-11 KR KR1019960064345A patent/KR100525146B1/ko not_active IP Right Cessation
- 1996-12-11 UA UA96124628A patent/UA35638C2/uk unknown
- 1996-12-11 BR BR9605968A patent/BR9605968A/pt not_active IP Right Cessation
- 1996-12-11 EE EE9600201A patent/EE03474B1/xx unknown
- 1996-12-11 SK SK1591-96A patent/SK282805B6/sk not_active IP Right Cessation
- 1996-12-11 RU RU96123410/04A patent/RU2162468C2/ru active
- 1996-12-11 SA SA96170492A patent/SA96170492B1/ar unknown
- 1996-12-11 NO NO19965298A patent/NO306725B1/no not_active IP Right Cessation
- 1996-12-11 CZ CZ19963646A patent/CZ288657B6/cs not_active IP Right Cessation
- 1996-12-12 SV SV1996000109A patent/SV1996000109A/es active IP Right Grant
- 1996-12-12 CN CN96123220A patent/CN1061348C/zh not_active Expired - Lifetime
- 1996-12-12 HU HU9603428A patent/HU226521B1/hu unknown
-
2002
- 2002-12-05 NL NL300109C patent/NL300109I1/nl unknown
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