PE33795A1 - Procedimiento en una etapa para la fabricacion de derivados de acido 3-quinoloncarboxilico - Google Patents
Procedimiento en una etapa para la fabricacion de derivados de acido 3-quinoloncarboxilicoInfo
- Publication number
- PE33795A1 PE33795A1 PE1994256625A PE25662594A PE33795A1 PE 33795 A1 PE33795 A1 PE 33795A1 PE 1994256625 A PE1994256625 A PE 1994256625A PE 25662594 A PE25662594 A PE 25662594A PE 33795 A1 PE33795 A1 PE 33795A1
- Authority
- PE
- Peru
- Prior art keywords
- formula
- chinoloncarboxylic
- manufacture
- acid derivatives
- coor
- Prior art date
Links
- UBIKHJZIEKPIBU-UHFFFAOYSA-N 3-oxo-2h-quinoline-2-carboxylic acid Chemical class C1=CC=CC2=CC(=O)C(C(=O)O)N=C21 UBIKHJZIEKPIBU-UHFFFAOYSA-N 0.000 title 1
- 238000004519 manufacturing process Methods 0.000 title 1
- 238000000034 method Methods 0.000 title 1
- 150000001875 compounds Chemical class 0.000 abstract 2
- 229910052736 halogen Inorganic materials 0.000 abstract 2
- 150000002367 halogens Chemical class 0.000 abstract 2
- BWHMMNNQKKPAPP-UHFFFAOYSA-L potassium carbonate Chemical compound [K+].[K+].[O-]C([O-])=O BWHMMNNQKKPAPP-UHFFFAOYSA-L 0.000 abstract 2
- 125000006519 CCH3 Chemical group 0.000 abstract 1
- -1 DIMETHYLAMIN ACRYLIC ACID ESTER Chemical class 0.000 abstract 1
- SECXISVLQFMRJM-UHFFFAOYSA-N N-Methylpyrrolidone Chemical compound CN1CCCC1=O SECXISVLQFMRJM-UHFFFAOYSA-N 0.000 abstract 1
- OCBFFGCSTGGPSQ-UHFFFAOYSA-N [CH2]CC Chemical class [CH2]CC OCBFFGCSTGGPSQ-UHFFFAOYSA-N 0.000 abstract 1
- XIPUIGPNIDKXJU-UHFFFAOYSA-N [CH]1CC1 Chemical class [CH]1CC1 XIPUIGPNIDKXJU-UHFFFAOYSA-N 0.000 abstract 1
- 239000002253 acid Substances 0.000 abstract 1
- 150000001412 amines Chemical class 0.000 abstract 1
- 230000000844 anti-bacterial effect Effects 0.000 abstract 1
- QUPDWYMUPZLYJZ-UHFFFAOYSA-N ethyl Chemical class C[CH2] QUPDWYMUPZLYJZ-UHFFFAOYSA-N 0.000 abstract 1
- 238000010438 heat treatment Methods 0.000 abstract 1
- 125000000956 methoxy group Chemical group [H]C([H])([H])O* 0.000 abstract 1
- WCYWZMWISLQXQU-UHFFFAOYSA-N methyl Chemical class [CH3] WCYWZMWISLQXQU-UHFFFAOYSA-N 0.000 abstract 1
- 229910000027 potassium carbonate Inorganic materials 0.000 abstract 1
- 239000002904 solvent Substances 0.000 abstract 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D487/00—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, not provided for by groups C07D451/00 - C07D477/00
- C07D487/02—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, not provided for by groups C07D451/00 - C07D477/00 in which the condensed system contains two hetero rings
- C07D487/04—Ortho-condensed systems
-
- 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
- C07D215/48—Carbon atoms having three bonds to hetero atoms with at the most one bond to halogen
- C07D215/54—Carbon atoms having three bonds to hetero atoms with at the most one bond to halogen attached in position 3
- C07D215/56—Carbon atoms having three bonds to hetero atoms with at the most one bond to halogen attached in position 3 with oxygen atoms in position 4
-
- 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
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Quinoline Compounds (AREA)
- Plural Heterocyclic Compounds (AREA)
- Nitrogen Condensed Heterocyclic Rings (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Nitrogen And Oxygen Or Sulfur-Condensed Heterocyclic Ring Systems (AREA)
- Agricultural Chemicals And Associated Chemicals (AREA)
- Materials For Photolithography (AREA)
Abstract
CARACTERIZADO POR COMPRENDER: 1) HACER REACCIONAR UN HALOGENURO DE ACIDO DE FORMULA XXVI DONDE HAL, X2 Y X3 SON F o Cl, CON: A) UN ESTER DE ACIDO DIMETILAMINOACRILICO DE FORMULA (CH3)2N-CH=CH-COOR, SEGUIDA POR LA ADICION DE UNA AMINA R1-NH2; o B) UN AMINOACRILESTER DE FORMULA R1NH-CH=CH-COOR; SIENDO R METILO, ETILO O PROPILO; 2) CALENTAR (1) A UNA TEMPERATURA DE 60°C A 100°C, EN UN DISOLVENTE COMO N-METILPIRROLIDONA CON UNA BASE AUXILIAR COMO CARBONATO DE POTASIO, FORMANDOSE UN CICLO NITROGENADO; 3) HACER REACCIONAR (2) CON UN COMPUESTO HETEROCICLICO R`R"N, FORMANDOSE UN COMPUESTO DE FORMULA I DONDE: R'R" JUNTO CON N FORMAN UN HETEROCICLO MONO O BICICLICO; A ES CH, CF, CCl, C-OCH3, C-CH3; X1 ES H, HALOGENO, NH2, CH3; R1 ES ALQUILO C1-C3, FCH2CH2-, CICLOPROPILO QUE PUEDE ESTAR SUSTITUIDO POR UNO A TRES HALOGENOS; EL CUAL ES UTIL COMO ANTIBACTERIANO
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
DE4342186A DE4342186A1 (de) | 1993-12-10 | 1993-12-10 | Eintopfverfahren zur Herstellung von 3-Chinoloncarbonsäurederivaten |
Publications (1)
Publication Number | Publication Date |
---|---|
PE33795A1 true PE33795A1 (es) | 1995-12-15 |
Family
ID=6504693
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
PE1994256625A PE33795A1 (es) | 1993-12-10 | 1994-12-07 | Procedimiento en una etapa para la fabricacion de derivados de acido 3-quinoloncarboxilico |
Country Status (35)
Country | Link |
---|---|
US (1) | US5639886A (es) |
EP (1) | EP0657448B1 (es) |
JP (1) | JP3963490B2 (es) |
KR (1) | KR950018008A (es) |
CN (1) | CN1109877A (es) |
AT (1) | ATE163645T1 (es) |
AU (1) | AU693818B2 (es) |
BG (1) | BG61947B1 (es) |
CA (1) | CA2137523C (es) |
CO (1) | CO4180607A1 (es) |
CZ (1) | CZ288078B6 (es) |
DE (2) | DE4342186A1 (es) |
DK (1) | DK0657448T3 (es) |
EE (1) | EE03215B1 (es) |
ES (1) | ES2113040T3 (es) |
FI (1) | FI945776A (es) |
GR (1) | GR3026383T3 (es) |
HR (1) | HRP940950B1 (es) |
HU (1) | HU220597B1 (es) |
IL (1) | IL111921A (es) |
LV (1) | LV11470B (es) |
MY (1) | MY113302A (es) |
NO (1) | NO307180B1 (es) |
NZ (1) | NZ270086A (es) |
PE (1) | PE33795A1 (es) |
PL (1) | PL180022B1 (es) |
RO (1) | RO113345B1 (es) |
RU (1) | RU2138483C1 (es) |
SI (1) | SI0657448T1 (es) |
SK (1) | SK279950B6 (es) |
SV (1) | SV1994000071A (es) |
TW (1) | TW401412B (es) |
UA (1) | UA41323C2 (es) |
YU (1) | YU48865B (es) |
ZA (1) | ZA949830B (es) |
Families Citing this family (25)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
DE19826050A1 (de) * | 1998-06-12 | 1999-12-16 | Bayer Ag | Verfahren zur Herstellung von Chinolon- und Naphthyridoncarbonsäuren und deren Ester |
KR20020075447A (ko) * | 2000-02-25 | 2002-10-04 | 다이이찌 세이야꾸 가부시기가이샤 | 퀴놀론카복실산의 제조방법 및 이의 중간체 |
US6608078B2 (en) | 2000-05-08 | 2003-08-19 | Wockhardt Limited | Antibacterial chiral 8-(substituted piperidino)-benzo [i,j] quinolizines, processes, compositions and methods of treatment |
DE10026903A1 (de) * | 2000-06-03 | 2002-01-10 | Cpc Cellular Process Chemistry | Verfahren zur Herstellung von Chinolon-3-carbonsäuren |
US7098219B2 (en) | 2000-08-01 | 2006-08-29 | Wockhart Limited | Inhibitors of cellular efflux pumps of microbes |
US6878713B2 (en) | 2001-04-25 | 2005-04-12 | Wockhardt Limited | Generation triple-targeting, chiral, broad-spectrum antimicrobial 7-substituted piperidino-quinolone carboxylic acid derivatives, their preparation, compositions and use as medicaments |
US6964966B2 (en) | 2001-04-25 | 2005-11-15 | Wockhardt Limited | Generation triple-targeting, chiral, broad-spectrum antimicrobial 7-substituted piperidino-quinolone carboxylic acid derivatives, their preparation, compositions and use as medicaments |
WO2003099815A1 (en) * | 2002-05-28 | 2003-12-04 | Wockhardt Limited | Crystalline fluoroquinolone arginine salt form |
KR100519158B1 (ko) * | 2002-12-21 | 2005-10-06 | 주식회사유한양행 | 퀴놀론 카르복실레이트 유도체의 제조방법 |
ATE366734T1 (de) | 2003-09-04 | 2007-08-15 | Wockhardt Ltd | Benzochinolizin-2-carbonsäureargininsalz- tetrahydrat |
WO2005026145A2 (en) * | 2003-09-12 | 2005-03-24 | Warner-Lambert Company Llc | Quinolone antibacterial agents |
CN100412075C (zh) * | 2004-06-22 | 2008-08-20 | 浙江医药股份有限公司新昌制药厂 | 左旋氧氟沙星和氧氟沙星的制备方法 |
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 |
FR2916446B1 (fr) * | 2007-05-24 | 2009-08-21 | Biocodex Sa | Nouveau procede de synthese de fluoroquinolones |
EP2083010A1 (en) | 2008-01-08 | 2009-07-29 | Chemo Ibérica, S.A. | Polymorphic Forms of Moxifloxacin hydrochloride and processes for preparation thereof |
CN101781299B (zh) * | 2010-01-13 | 2012-06-27 | 杭州师范大学 | 一种喹诺酮类药物关键中间体的一锅法合成方法 |
IT1398952B1 (it) * | 2010-03-19 | 2013-03-28 | F S I Fabbrica Italiana Sint | Processo di preparazione della moxifloxacina e suoi sali |
CN102675306A (zh) * | 2011-03-17 | 2012-09-19 | 苏州中科天马肽工程中心有限公司 | 一种莫西沙星或其盐的制备方法 |
CN102267994B (zh) * | 2011-06-17 | 2013-01-30 | 江苏正大丰海制药有限公司 | 一种盐酸莫西沙星已知杂质的制备方法 |
WO2013157018A1 (en) | 2012-04-18 | 2013-10-24 | Indian Institute Of Technology Madras | A process for the preparation of the core structure in quinolone and napthyridone class of antibiotics |
US9388178B2 (en) | 2012-12-04 | 2016-07-12 | Mankind Research Centre | Process for the preparation of moxifloxacin hydrochloride |
UA106556C2 (uk) | 2013-05-13 | 2014-09-10 | Наталья Николаевна Деркач | СПОСІБ ОДЕРЖАННЯ (1-ЦИКЛОПРОПІЛ-6-ФТОР-1,4-ДИГІДРО-8-МЕТОКСІ-7-[(4aS,7aS)-ОКТАГІДРО-6Н-ПІРОЛО[3,4-b]-4-ОКСО-3-ХІНОЛІНКАРБОНОВОЇ КИСЛОТИ |
US11059788B2 (en) | 2017-06-12 | 2021-07-13 | Virginia Commonwealth University | Streamlined syntheses of fluoroquinolones |
CN115385856A (zh) * | 2022-09-05 | 2022-11-25 | 常州大学 | 一锅法合成诺氟沙星中间体的方法 |
Family Cites Families (13)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US5468861A (en) * | 1984-06-04 | 1995-11-21 | Bayer Aktiengesellschaft | 8-chloro-1-cyclopropyl-6,7-difluoro-1,4-dihydro-4-oxo-3-quinolinecarboxylic acid and alkyl esters thereof |
DE3420743A1 (de) | 1984-06-04 | 1985-12-05 | Bayer Ag, 5090 Leverkusen | 7-amino-1-cyclopropyl-6,8-dihalogen-1,4-dihydro-4-oxo-3-chinolincarbonsaeuren, verfahren zu ihrer herstellung sowie diese enthaltende antibakterielle mittel |
JPS62215572A (ja) * | 1986-03-17 | 1987-09-22 | Kyorin Pharmaceut Co Ltd | キノロンカルボン酸誘導体 |
JPS63179856A (ja) | 1987-01-21 | 1988-07-23 | Kyorin Pharmaceut Co Ltd | キノロンカルボン酸誘導体の製造方法並びにその中間体 |
DE3724466A1 (de) | 1987-07-24 | 1989-02-02 | Bayer Ag | Verfahren zur herstellung von chinoloncarbonsaeuren |
US4780468A (en) * | 1987-08-07 | 1988-10-25 | Warner-Lambert Company | 8-trifluoromethyl quinolones as antibacterial agents |
WO1989005643A1 (en) * | 1987-12-18 | 1989-06-29 | Pfizer Inc. | Heterocyclic-substituted quinoline-carboxylic acids |
DE3906365A1 (de) * | 1988-07-15 | 1990-01-18 | Bayer Ag | 7-(1-pyrrolidinyl)-3-chinolon- und -naphthyridoncarbonsaeure-derivate, verfahren sowie substituierte (oxa)diazabicyclooctane und -nonane als zwischenprodukte zu ihrer herstellung, und sie enthaltende antibakterielle mittel und futterzusatzstoffe |
TW209865B (es) * | 1992-01-10 | 1993-07-21 | Bayer Ag | |
DE4208789A1 (de) | 1992-03-19 | 1993-09-23 | Bayer Ag | Enantiomerenreine chinolincarbonsaeure-derivate |
DE4208792A1 (de) | 1992-03-19 | 1993-09-23 | Bayer Ag | Enantiomerenreine chinolincarbonsaeure-derivate |
AU4272793A (en) * | 1993-04-24 | 1994-11-21 | Korea Research Institute Of Chemical Technology | Novel quinolone carboxylic acid derivatives and process for preparing the same |
JP2758722B2 (ja) * | 1993-08-13 | 1998-05-28 | ドング ホワ ファーマシューチカル インダストリアル カンパニー,リミテッド | 新規キノロンカルボン酸誘導体 |
-
1993
- 1993-12-10 DE DE4342186A patent/DE4342186A1/de not_active Withdrawn
-
1994
- 1994-11-18 EE EE9400332A patent/EE03215B1/xx not_active IP Right Cessation
- 1994-11-21 TW TW083110792A patent/TW401412B/zh not_active IP Right Cessation
- 1994-11-23 HR HRP4342186.5A patent/HRP940950B1/xx not_active IP Right Cessation
- 1994-11-28 EP EP94118676A patent/EP0657448B1/de not_active Expired - Lifetime
- 1994-11-28 DE DE59405376T patent/DE59405376D1/de not_active Expired - Lifetime
- 1994-11-28 DK DK94118676T patent/DK0657448T3/da active
- 1994-11-28 CO CO94054149A patent/CO4180607A1/es unknown
- 1994-11-28 SI SI9430120T patent/SI0657448T1/xx unknown
- 1994-11-28 AT AT94118676T patent/ATE163645T1/de not_active IP Right Cessation
- 1994-11-28 ES ES94118676T patent/ES2113040T3/es not_active Expired - Lifetime
- 1994-12-02 US US08/348,400 patent/US5639886A/en not_active Expired - Lifetime
- 1994-12-05 JP JP32920694A patent/JP3963490B2/ja not_active Expired - Lifetime
- 1994-12-06 RO RO94-01949A patent/RO113345B1/ro unknown
- 1994-12-06 AU AU80244/94A patent/AU693818B2/en not_active Ceased
- 1994-12-07 SK SK1514-94A patent/SK279950B6/sk unknown
- 1994-12-07 PE PE1994256625A patent/PE33795A1/es not_active Application Discontinuation
- 1994-12-07 NZ NZ270086A patent/NZ270086A/en unknown
- 1994-12-07 IL IL11192194A patent/IL111921A/xx not_active IP Right Cessation
- 1994-12-07 CA CA002137523A patent/CA2137523C/en not_active Expired - Lifetime
- 1994-12-08 SV SV1994000071A patent/SV1994000071A/es not_active Application Discontinuation
- 1994-12-08 BG BG99248A patent/BG61947B1/bg unknown
- 1994-12-08 FI FI945776A patent/FI945776A/fi unknown
- 1994-12-08 YU YU71694A patent/YU48865B/sh unknown
- 1994-12-09 CZ CZ19943105A patent/CZ288078B6/cs not_active IP Right Cessation
- 1994-12-09 UA UA94129157A patent/UA41323C2/uk unknown
- 1994-12-09 KR KR1019940033433A patent/KR950018008A/ko not_active Application Discontinuation
- 1994-12-09 RU RU94043645A patent/RU2138483C1/ru active
- 1994-12-09 PL PL94306198A patent/PL180022B1/pl unknown
- 1994-12-09 MY MYPI94003290A patent/MY113302A/en unknown
- 1994-12-09 NO NO944786A patent/NO307180B1/no not_active IP Right Cessation
- 1994-12-09 ZA ZA949830A patent/ZA949830B/xx unknown
- 1994-12-09 LV LVP-94-241A patent/LV11470B/lv unknown
- 1994-12-09 CN CN94112890A patent/CN1109877A/zh active Pending
- 1994-12-09 HU HU9403553A patent/HU220597B1/hu not_active IP Right Cessation
-
1998
- 1998-03-17 GR GR980400579T patent/GR3026383T3/el unknown
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Legal Events
Date | Code | Title | Description |
---|---|---|---|
FG | Grant, registration | ||
FD | Application declared void or lapsed |