RU94015601A - Способ получения энантиомеров арилалкановых кислот - Google Patents
Способ получения энантиомеров арилалкановых кислотInfo
- Publication number
- RU94015601A RU94015601A RU94015601/13A RU94015601A RU94015601A RU 94015601 A RU94015601 A RU 94015601A RU 94015601/13 A RU94015601/13 A RU 94015601/13A RU 94015601 A RU94015601 A RU 94015601A RU 94015601 A RU94015601 A RU 94015601A
- Authority
- RU
- Russia
- Prior art keywords
- synthesis
- arylalkanoic acid
- acid enantiomers
- ketoprofen
- arylalkanoic
- Prior art date
Links
- 239000002253 acid Substances 0.000 title claims abstract 3
- HBAQYPYDRFILMT-UHFFFAOYSA-N 8-[3-(1-cyclopropylpyrazol-4-yl)-1H-pyrazolo[4,3-d]pyrimidin-5-yl]-3-methyl-3,8-diazabicyclo[3.2.1]octan-2-one Chemical class C1(CC1)N1N=CC(=C1)C1=NNC2=C1N=C(N=C2)N1C2C(N(CC1CC2)C)=O HBAQYPYDRFILMT-UHFFFAOYSA-N 0.000 title 1
- 230000015572 biosynthetic process Effects 0.000 title 1
- 238000000034 method Methods 0.000 title 1
- 238000003786 synthesis reaction Methods 0.000 title 1
- 150000007513 acids Chemical class 0.000 claims abstract 2
- 230000036983 biotransformation Effects 0.000 claims abstract 2
- DKYWVDODHFEZIM-NSHDSACASA-N dexketoprofen Chemical compound OC(=O)[C@@H](C)C1=CC=CC(C(=O)C=2C=CC=CC=2)=C1 DKYWVDODHFEZIM-NSHDSACASA-N 0.000 claims abstract 2
- 229960002783 dexketoprofen Drugs 0.000 claims abstract 2
- CQSMNXCTDMLMLM-UHFFFAOYSA-N ethyl 2-(3-benzoylphenyl)propanoate Chemical compound CCOC(=O)C(C)C1=CC=CC(C(=O)C=2C=CC=CC=2)=C1 CQSMNXCTDMLMLM-UHFFFAOYSA-N 0.000 claims abstract 2
- 244000005700 microbiome Species 0.000 claims abstract 2
- 239000000203 mixture Substances 0.000 claims abstract 2
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D213/00—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members
- C07D213/02—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members
- C07D213/04—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen or carbon atoms directly attached to the ring nitrogen atom
- C07D213/24—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen or carbon atoms directly attached to the ring nitrogen atom with substituted hydrocarbon radicals attached to ring carbon atoms
- C07D213/54—Radicals substituted by carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals
- C07D213/55—Acids; Esters
-
- 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
-
- C—CHEMISTRY; METALLURGY
- C12—BIOCHEMISTRY; BEER; SPIRITS; WINE; VINEGAR; MICROBIOLOGY; ENZYMOLOGY; MUTATION OR GENETIC ENGINEERING
- C12P—FERMENTATION OR ENZYME-USING PROCESSES TO SYNTHESISE A DESIRED CHEMICAL COMPOUND OR COMPOSITION OR TO SEPARATE OPTICAL ISOMERS FROM A RACEMIC MIXTURE
- C12P17/00—Preparation of heterocyclic carbon compounds with only O, N, S, Se or Te as ring hetero atoms
- C12P17/10—Nitrogen as only ring hetero atom
- C12P17/12—Nitrogen as only ring hetero atom containing a six-membered hetero ring
-
- C—CHEMISTRY; METALLURGY
- C12—BIOCHEMISTRY; BEER; SPIRITS; WINE; VINEGAR; MICROBIOLOGY; ENZYMOLOGY; MUTATION OR GENETIC ENGINEERING
- C12P—FERMENTATION OR ENZYME-USING PROCESSES TO SYNTHESISE A DESIRED CHEMICAL COMPOUND OR COMPOSITION OR TO SEPARATE OPTICAL ISOMERS FROM A RACEMIC MIXTURE
- C12P41/00—Processes using enzymes or microorganisms to separate optical isomers from a racemic mixture
- C12P41/003—Processes using enzymes or microorganisms to separate optical isomers from a racemic mixture by ester formation, lactone formation or the inverse reactions
- C12P41/005—Processes using enzymes or microorganisms to separate optical isomers from a racemic mixture by ester formation, lactone formation or the inverse reactions by esterification of carboxylic acid groups in the enantiomers or the inverse reaction
-
- C—CHEMISTRY; METALLURGY
- C12—BIOCHEMISTRY; BEER; SPIRITS; WINE; VINEGAR; MICROBIOLOGY; ENZYMOLOGY; MUTATION OR GENETIC ENGINEERING
- C12P—FERMENTATION OR ENZYME-USING PROCESSES TO SYNTHESISE A DESIRED CHEMICAL COMPOUND OR COMPOSITION OR TO SEPARATE OPTICAL ISOMERS FROM A RACEMIC MIXTURE
- C12P7/00—Preparation of oxygen-containing organic compounds
- C12P7/40—Preparation of oxygen-containing organic compounds containing a carboxyl group including Peroxycarboxylic acids
-
- C—CHEMISTRY; METALLURGY
- C12—BIOCHEMISTRY; BEER; SPIRITS; WINE; VINEGAR; MICROBIOLOGY; ENZYMOLOGY; MUTATION OR GENETIC ENGINEERING
- C12P—FERMENTATION OR ENZYME-USING PROCESSES TO SYNTHESISE A DESIRED CHEMICAL COMPOUND OR COMPOSITION OR TO SEPARATE OPTICAL ISOMERS FROM A RACEMIC MIXTURE
- C12P7/00—Preparation of oxygen-containing organic compounds
- C12P7/40—Preparation of oxygen-containing organic compounds containing a carboxyl group including Peroxycarboxylic acids
- C12P7/44—Polycarboxylic acids
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Engineering & Computer Science (AREA)
- Life Sciences & Earth Sciences (AREA)
- Zoology (AREA)
- Wood Science & Technology (AREA)
- Health & Medical Sciences (AREA)
- General Engineering & Computer Science (AREA)
- General Chemical & Material Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Biotechnology (AREA)
- Biochemistry (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Microbiology (AREA)
- General Health & Medical Sciences (AREA)
- Genetics & Genomics (AREA)
- Analytical Chemistry (AREA)
- Preparation Of Compounds By Using Micro-Organisms (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Acyclic And Carbocyclic Compounds In Medicinal Compositions (AREA)
- Micro-Organisms Or Cultivation Processes Thereof (AREA)
Abstract
Используя подходящий микроорганизм, получают в процессе биотрансформации арилалкановые кислоты и, в частности, (S)-кетопрофен с чистотой более 95% из рацемической смеси этилового эфира кетопрофена.
Claims (1)
- Используя подходящий микроорганизм, получают в процессе биотрансформации арилалкановые кислоты и, в частности, (S)-кетопрофен с чистотой более 95% из рацемической смеси этилового эфира кетопрофена.
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| GB919118149A GB9118149D0 (en) | 1991-08-22 | 1991-08-22 | Araylalkanoic acid resolution |
| GB9118149.5 | 1991-08-22 |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| RU94015601A true RU94015601A (ru) | 1996-07-10 |
| RU2119955C1 RU2119955C1 (ru) | 1998-10-10 |
Family
ID=10700381
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| RU94015601A RU2119955C1 (ru) | 1991-08-22 | 1992-08-19 | Способ получения (s)-кетопрофена |
Country Status (22)
| Country | Link |
|---|---|
| US (1) | US5516690A (ru) |
| EP (1) | EP0599967B1 (ru) |
| JP (1) | JP3174328B2 (ru) |
| KR (1) | KR100240696B1 (ru) |
| AT (1) | ATE161053T1 (ru) |
| AU (1) | AU662556B2 (ru) |
| BG (1) | BG62056B1 (ru) |
| CA (1) | CA2116003C (ru) |
| CZ (1) | CZ283141B6 (ru) |
| DE (2) | DE69223516T2 (ru) |
| DK (1) | DK0599967T3 (ru) |
| ES (1) | ES2058047T3 (ru) |
| FI (1) | FI103807B (ru) |
| GB (1) | GB9118149D0 (ru) |
| GR (2) | GR940300068T1 (ru) |
| HU (1) | HU213748B (ru) |
| NO (1) | NO315750B1 (ru) |
| RO (1) | RO115970B1 (ru) |
| RU (1) | RU2119955C1 (ru) |
| SK (1) | SK280179B6 (ru) |
| UA (1) | UA27817C2 (ru) |
| WO (1) | WO1993004189A1 (ru) |
Cited By (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| RU2646829C1 (ru) * | 2013-12-16 | 2018-03-07 | ЗОИТИС СЕРВИСЕЗ ЭлЭлСи | Композиции длительного действия на основе кетопрофена |
Families Citing this family (8)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| GB9304256D0 (en) * | 1993-03-03 | 1993-04-21 | Chiros Ltd | Arylalkanoic acid resolution |
| GB9304351D0 (en) * | 1993-03-03 | 1993-04-21 | Chiros Ltd | Arylalkanoic acid resolution and microorganisms for use therein |
| US5912164A (en) * | 1993-03-03 | 1999-06-15 | Laboratorios Menarini S.A. | Stereoselective hydrolysis of chiral carboxylic acid esters using esterase from ophiostoma or ceratocystis |
| US6242243B1 (en) * | 1998-03-30 | 2001-06-05 | Council Of Scientific & Industrial Research | Trichosporon sp RRLY-15 (DSM 11829) and its use to prepare S(+)-6-methoxy-methyl-2-naphthalene acetic acid |
| US20030059903A1 (en) * | 2001-04-03 | 2003-03-27 | Degussa Ag | Process for the production of L-amino acids using strains of the family enterobacteriaceae that contain an attenuated aceA gene |
| US7223582B2 (en) * | 2002-01-17 | 2007-05-29 | Korea Research Institute Of Bioscience And Biotechnology | Esterase, its DNA, its overexpression and production of optically active aryl propionic acids using the same |
| RU2290758C1 (ru) * | 2005-04-25 | 2006-12-27 | Федеральное государственное унитарное предприятие "Воронежский научно-исследовательский институт связи" | Способ передачи дискретной информации в радиолинии со скачкообразной перестройкой рабочей частоты |
| RU2364442C1 (ru) * | 2008-06-30 | 2009-08-20 | Государственное образовательное учреждение высшего профессионального образования "Тверской государственный технический университет" | Способ приготовления модифицированного платинового катализатора для энантиоселективного гидрирования сложных эфиров альфа-кетокарбоновых кислот |
Family Cites Families (6)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| DE3680132D1 (de) * | 1985-04-01 | 1991-08-14 | Kanegafuchi Chemical Ind | Verfahren zur herstellung von optisch aktiver indolin-2-carbonsaeure. |
| US5322791A (en) * | 1985-12-20 | 1994-06-21 | Wisconsin Alumni Research Foundation | Process for preparing (S)-α-methylarylacetic acids |
| AU599944B2 (en) * | 1985-12-20 | 1990-08-02 | Wisconsin Alumni Research Foundation | Process for preparing (S)-alpha-methylarylacetic acids |
| US4857469A (en) * | 1987-04-09 | 1989-08-15 | Toyo Jozo Co., Ltd. | Process for preparing optically active mercapto compound |
| US5108916A (en) * | 1989-06-05 | 1992-04-28 | Rhone-Poulenc Rorer, S.A. | Process for stereoselectively hydrolyzing, transesterifying or esterifying with immobilized isozyme of lipase from candida rugosa |
| CA2076972A1 (en) * | 1990-02-26 | 1991-08-27 | Animesh Goswami | Stereospecific resolution by hydrolysis of esters of 2-arylpropionic acids by liver enzymes |
-
1991
- 1991-08-22 GB GB919118149A patent/GB9118149D0/en active Pending
-
1992
- 1992-08-19 EP EP92918204A patent/EP0599967B1/en not_active Expired - Lifetime
- 1992-08-19 DK DK92918204T patent/DK0599967T3/da active
- 1992-08-19 DE DE69223516T patent/DE69223516T2/de not_active Expired - Lifetime
- 1992-08-19 JP JP51163292A patent/JP3174328B2/ja not_active Expired - Lifetime
- 1992-08-19 KR KR1019940700492A patent/KR100240696B1/ko not_active Expired - Lifetime
- 1992-08-19 WO PCT/EP1992/001892 patent/WO1993004189A1/en not_active Ceased
- 1992-08-19 CA CA002116003A patent/CA2116003C/en not_active Expired - Lifetime
- 1992-08-19 UA UA94005318A patent/UA27817C2/uk unknown
- 1992-08-19 US US08/193,004 patent/US5516690A/en not_active Expired - Lifetime
- 1992-08-19 DE DE0599967T patent/DE599967T1/de active Pending
- 1992-08-19 AU AU24685/92A patent/AU662556B2/en not_active Expired
- 1992-08-19 CZ CZ94364A patent/CZ283141B6/cs not_active IP Right Cessation
- 1992-08-19 ES ES92918204T patent/ES2058047T3/es not_active Expired - Lifetime
- 1992-08-19 HU HU9400462A patent/HU213748B/hu unknown
- 1992-08-19 AT AT92918204T patent/ATE161053T1/de active
- 1992-08-19 RO RO94-00247A patent/RO115970B1/ro unknown
- 1992-08-19 RU RU94015601A patent/RU2119955C1/ru active
- 1992-08-19 SK SK176-94A patent/SK280179B6/sk not_active IP Right Cessation
-
1994
- 1994-02-16 BG BG98484A patent/BG62056B1/bg unknown
- 1994-02-18 NO NO19940570A patent/NO315750B1/no not_active IP Right Cessation
- 1994-02-18 FI FI940792A patent/FI103807B/fi not_active IP Right Cessation
- 1994-10-31 GR GR940300068T patent/GR940300068T1/el unknown
-
1998
- 1998-03-06 GR GR980400474T patent/GR3026303T3/el unknown
Cited By (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| RU2646829C1 (ru) * | 2013-12-16 | 2018-03-07 | ЗОИТИС СЕРВИСЕЗ ЭлЭлСи | Композиции длительного действия на основе кетопрофена |
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