SK284810B6 - Spôsob výroby (1S,4R)- alebo (1R,4S)-4-(2-amino-6-chlór-9-H- purín-9-yl)-2-cyklopentén-1-metanolu - Google Patents
Spôsob výroby (1S,4R)- alebo (1R,4S)-4-(2-amino-6-chlór-9-H- purín-9-yl)-2-cyklopentén-1-metanolu Download PDFInfo
- Publication number
- SK284810B6 SK284810B6 SK589-98A SK58998A SK284810B6 SK 284810 B6 SK284810 B6 SK 284810B6 SK 58998 A SK58998 A SK 58998A SK 284810 B6 SK284810 B6 SK 284810B6
- Authority
- SK
- Slovakia
- Prior art keywords
- amino
- cyclopentene
- carried out
- process according
- formula
- Prior art date
Links
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D473/00—Heterocyclic compounds containing purine ring systems
- C07D473/26—Heterocyclic compounds containing purine ring systems with an oxygen, sulphur, or nitrogen atom directly attached in position 2 or 6, but not in both
- C07D473/32—Nitrogen atom
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C231/00—Preparation of carboxylic acid amides
- C07C231/16—Preparation of optical isomers
- C07C231/18—Preparation of optical isomers by stereospecific synthesis
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C233/00—Carboxylic acid amides
- C07C233/01—Carboxylic acid amides having carbon atoms of carboxamide groups bound to hydrogen atoms or to acyclic carbon atoms
- C07C233/16—Carboxylic acid amides having carbon atoms of carboxamide groups bound to hydrogen atoms or to acyclic carbon atoms having the nitrogen atom of at least one of the carboxamide groups bound to a carbon atom of a hydrocarbon radical substituted by singly-bound oxygen atoms
- C07C233/23—Carboxylic acid amides having carbon atoms of carboxamide groups bound to hydrogen atoms or to acyclic carbon atoms having the nitrogen atom of at least one of the carboxamide groups bound to a carbon atom of a hydrocarbon radical substituted by singly-bound oxygen atoms with the substituted hydrocarbon radical bound to the nitrogen atom of the carboxamide group by a carbon atom of a ring other than a six-membered aromatic ring
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C271/00—Derivatives of carbamic acids, i.e. compounds containing any of the groups, the nitrogen atom not being part of nitro or nitroso groups
- C07C271/06—Esters of carbamic acids
- C07C271/08—Esters of carbamic acids having oxygen atoms of carbamate groups bound to acyclic carbon atoms
- C07C271/24—Esters of carbamic acids having oxygen atoms of carbamate groups bound to acyclic carbon atoms with the nitrogen atom of at least one of the carbamate groups bound to a carbon atom of a ring other than a six-membered aromatic ring
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D209/00—Heterocyclic compounds containing five-membered rings, condensed with other rings, with one nitrogen atom as the only ring hetero atom
- C07D209/56—Ring systems containing three or more rings
- C07D209/80—[b, c]- or [b, d]-condensed
- C07D209/94—[b, c]- or [b, d]-condensed containing carbocyclic rings other than six-membered
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D473/00—Heterocyclic compounds containing purine ring systems
- C07D473/40—Heterocyclic compounds containing purine ring systems with halogen atoms or perhalogeno-alkyl radicals directly attached in position 2 or 6
-
- 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
- C12P13/00—Preparation of nitrogen-containing organic compounds
- C12P13/001—Amines; Imines
-
- 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
- C12P13/00—Preparation of nitrogen-containing organic compounds
- C12P13/02—Amides, e.g. chloramphenicol or polyamides; Imides or polyimides; Urethanes, i.e. compounds comprising N-C=O structural element or polyurethanes
-
- 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
- C12P17/18—Preparation of heterocyclic carbon compounds with only O, N, S, Se or Te as ring hetero atoms containing at least two hetero rings condensed among themselves or condensed with a common carbocyclic ring system, e.g. rifamycin
- C12P17/182—Heterocyclic compounds containing nitrogen atoms as the only ring heteroatoms in the condensed system
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07B—GENERAL METHODS OF ORGANIC CHEMISTRY; APPARATUS THEREFOR
- C07B2200/00—Indexing scheme relating to specific properties of organic compounds
- C07B2200/07—Optical isomers
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C2601/00—Systems containing only non-condensed rings
- C07C2601/06—Systems containing only non-condensed rings with a five-membered ring
- C07C2601/10—Systems containing only non-condensed rings with a five-membered ring the ring being unsaturated
Landscapes
- Organic Chemistry (AREA)
- Chemical & Material Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- Engineering & Computer Science (AREA)
- Zoology (AREA)
- Wood Science & Technology (AREA)
- Biochemistry (AREA)
- General Health & Medical Sciences (AREA)
- General Chemical & Material Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Biotechnology (AREA)
- Health & Medical Sciences (AREA)
- Genetics & Genomics (AREA)
- Bioinformatics & Cheminformatics (AREA)
- General Engineering & Computer Science (AREA)
- Microbiology (AREA)
- Proteomics, Peptides & Aminoacids (AREA)
- Preparation Of Compounds By Using Micro-Organisms (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Indole Compounds (AREA)
- Peptides Or Proteins (AREA)
- Low-Molecular Organic Synthesis Reactions Using Catalysts (AREA)
- Micro-Organisms Or Cultivation Processes Thereof (AREA)
- Nitrogen Condensed Heterocyclic Rings (AREA)
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
CH111697 | 1997-05-13 | ||
CH274097 | 1997-11-27 |
Publications (2)
Publication Number | Publication Date |
---|---|
SK58998A3 SK58998A3 (en) | 1998-12-02 |
SK284810B6 true SK284810B6 (sk) | 2005-12-01 |
Family
ID=25686703
Family Applications (3)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
SK53-2005A SK285228B6 (sk) | 1997-05-13 | 1998-05-04 | Spôsob výroby racemického alebo opticky aktívnehoderivátu 4-(hydroxymetyl)-2-cyklopenténu a racemicky N-butyryl-1-amino-4- (hydroxymetyl)-2-cyklopentén |
SK54-2005A SK285229B6 (sk) | 1997-05-13 | 1998-05-04 | Spôsob výroby derivátov (1R,4S)- alebo (1S,4R)-1-amino-4- (hydroxymetyl)-2-cyklopenténu a enantioméru (1R,4S)-N-butyryl-1- amino-4-(hydroxymetyl)-2-cyklopenténu |
SK589-98A SK284810B6 (sk) | 1997-05-13 | 1998-05-04 | Spôsob výroby (1S,4R)- alebo (1R,4S)-4-(2-amino-6-chlór-9-H- purín-9-yl)-2-cyklopentén-1-metanolu |
Family Applications Before (2)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
SK53-2005A SK285228B6 (sk) | 1997-05-13 | 1998-05-04 | Spôsob výroby racemického alebo opticky aktívnehoderivátu 4-(hydroxymetyl)-2-cyklopenténu a racemicky N-butyryl-1-amino-4- (hydroxymetyl)-2-cyklopentén |
SK54-2005A SK285229B6 (sk) | 1997-05-13 | 1998-05-04 | Spôsob výroby derivátov (1R,4S)- alebo (1S,4R)-1-amino-4- (hydroxymetyl)-2-cyklopenténu a enantioméru (1R,4S)-N-butyryl-1- amino-4-(hydroxymetyl)-2-cyklopenténu |
Country Status (17)
Country | Link |
---|---|
US (4) | US6156893A (zh) |
EP (2) | EP1502914A1 (zh) |
JP (3) | JP4540136B2 (zh) |
KR (2) | KR100577886B1 (zh) |
CN (2) | CN1302116C (zh) |
AT (1) | ATE275206T1 (zh) |
CA (1) | CA2237297C (zh) |
CZ (3) | CZ297894B6 (zh) |
DE (1) | DE59811884D1 (zh) |
DK (1) | DK0878548T3 (zh) |
ES (1) | ES2223095T3 (zh) |
HK (1) | HK1092782A1 (zh) |
HU (1) | HU226327B1 (zh) |
NO (1) | NO324679B1 (zh) |
PL (1) | PL197848B1 (zh) |
PT (1) | PT878548E (zh) |
SK (3) | SK285228B6 (zh) |
Families Citing this family (10)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
DK0705263T3 (da) * | 1993-06-21 | 1997-05-05 | Merrell Pharma Inc | Carbocycliske nukleoside midler anvendelige som selektive inhibitorer af proinflammatoriske cytokiner |
GB9717928D0 (en) * | 1997-08-22 | 1997-10-29 | Glaxo Group Ltd | Process for the enatioselective hydrolysis of n-derivatised lactams |
GB9721780D0 (en) * | 1997-10-14 | 1997-12-10 | Glaxo Group Ltd | Process for the synthesis of chloropurine intermediates |
SK284596B6 (sk) * | 1997-11-27 | 2005-07-01 | Lonza Ag | Spôsob výroby (1S,4R)- alebo (1R,4S)-4-(2-amino-6-chlór-9-H- purin-9-yl)-2-cyklopentén-1-metanolu alebo jeho solí |
PL196857B1 (pl) * | 1998-12-23 | 2008-02-29 | Lonza Ag | Sposób wytwarzania enancjomerycznie wzbogaconych pochodnych 1-amino-4- (hydroksymetylo)-cyklopent-2-enu oraz 1-amino-4-(hydroksymetylo)-cyklopent-2-enów |
KR101120813B1 (ko) * | 2003-07-25 | 2012-03-23 | 프로메틱 바이오사이언시즈 인코포레이티드 | 중-쇄 지방산 금속염의 제조 방법 |
DE102005061756B4 (de) * | 2005-12-21 | 2008-01-03 | Sanofi-Aventis Deutschland Gmbh | Verbessertes Verfahren zur Herstellung von Ramipril |
US8236853B1 (en) | 2007-12-03 | 2012-08-07 | University Of South Florida | Formation of cyclopentene nitro-ester and derivatives |
WO2012099904A1 (en) | 2011-01-18 | 2012-07-26 | General Atomics | Hydrolase enzyme substrates and uses thereof |
CN102557990B (zh) * | 2011-04-25 | 2014-06-25 | 开原亨泰制药股份有限公司 | (1s,4r)n-叔丁氧羰基-4-氨基-2-环戊烯-1-羧酸甲酯的制备方法 |
Family Cites Families (12)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US4931559A (en) * | 1988-01-20 | 1990-06-05 | Regents Of The University Of Minnesota | Optically-active isomers of dideoxycarbocyclic nucleosides |
US4950758A (en) * | 1988-01-20 | 1990-08-21 | Regents Of The University Of Minnesota | Optically-active isomers of dideoxycarbocyclic nucleosides |
MY104575A (en) * | 1989-12-22 | 1994-04-30 | The Wellcome Foundation Ltd | Therapeutic nucleosides. |
CA2055086A1 (en) * | 1991-02-12 | 1992-08-13 | Chikara Kaneko | Cyclopentene derivatives and their use |
US5200527A (en) * | 1991-04-08 | 1993-04-06 | Lonza Ltd. | Process for the production of 2-azabicyclo [2.2.1] hept-5-en-3-one |
GB9204015D0 (en) * | 1992-02-25 | 1992-04-08 | Wellcome Found | Therapeutic nucleosides |
GB9205071D0 (en) * | 1992-03-09 | 1992-04-22 | Wellcome Found | Therapeutic nucleosides |
GB9217823D0 (en) * | 1992-08-21 | 1992-10-07 | Glaxo Group Ltd | Chemical process |
JPH06116217A (ja) * | 1992-10-02 | 1994-04-26 | Kuraray Co Ltd | (±)−シス−4−アミノシクロペント−2−エンカルボン酸誘導体の光学分割法 |
GB9402161D0 (en) * | 1994-02-04 | 1994-03-30 | Wellcome Found | Chloropyrimidine intermediates |
ATE283348T1 (de) * | 1996-05-30 | 2004-12-15 | Lonza Ag | Verfahren zur herstellung von aminoalkoholen und derivaten davon |
GB9625455D0 (en) * | 1996-12-07 | 1997-01-22 | Glaxo Group Ltd | Process for resolving mixtures of carbocyclic steroisomers |
-
1998
- 1998-05-04 SK SK53-2005A patent/SK285228B6/sk not_active IP Right Cessation
- 1998-05-04 SK SK54-2005A patent/SK285229B6/sk not_active IP Right Cessation
- 1998-05-04 SK SK589-98A patent/SK284810B6/sk not_active IP Right Cessation
- 1998-05-06 US US09/073,553 patent/US6156893A/en not_active Expired - Fee Related
- 1998-05-11 KR KR1019980016803A patent/KR100577886B1/ko not_active IP Right Cessation
- 1998-05-11 CA CA002237297A patent/CA2237297C/en not_active Expired - Fee Related
- 1998-05-11 CZ CZ0145898A patent/CZ297894B6/cs not_active IP Right Cessation
- 1998-05-11 CZ CZ20060695A patent/CZ297888B6/cs not_active IP Right Cessation
- 1998-05-11 CZ CZ20060694A patent/CZ297887B6/cs not_active IP Right Cessation
- 1998-05-12 NO NO19982149A patent/NO324679B1/no not_active IP Right Cessation
- 1998-05-12 JP JP12933898A patent/JP4540136B2/ja not_active Expired - Fee Related
- 1998-05-13 DE DE59811884T patent/DE59811884D1/de not_active Expired - Lifetime
- 1998-05-13 EP EP04020273A patent/EP1502914A1/de not_active Withdrawn
- 1998-05-13 DK DK98108721T patent/DK0878548T3/da active
- 1998-05-13 ES ES98108721T patent/ES2223095T3/es not_active Expired - Lifetime
- 1998-05-13 EP EP98108721A patent/EP0878548B1/de not_active Expired - Lifetime
- 1998-05-13 AT AT98108721T patent/ATE275206T1/de active
- 1998-05-13 CN CNB03123433XA patent/CN1302116C/zh not_active Expired - Fee Related
- 1998-05-13 PL PL326267A patent/PL197848B1/pl not_active IP Right Cessation
- 1998-05-13 HU HU9801083A patent/HU226327B1/hu not_active IP Right Cessation
- 1998-05-13 PT PT98108721T patent/PT878548E/pt unknown
- 1998-05-13 CN CN98108865A patent/CN1115343C/zh not_active Expired - Fee Related
-
1999
- 1999-08-13 US US09/373,862 patent/US6137007A/en not_active Expired - Fee Related
- 1999-08-13 US US09/373,856 patent/US6262295B1/en not_active Expired - Fee Related
- 1999-08-13 US US09/373,857 patent/US6252112B1/en not_active Expired - Fee Related
-
2005
- 2005-10-19 KR KR1020050098642A patent/KR100601764B1/ko not_active IP Right Cessation
-
2006
- 2006-12-07 HK HK06113474.2A patent/HK1092782A1/xx not_active IP Right Cessation
-
2009
- 2009-11-09 JP JP2009256399A patent/JP2010106025A/ja active Pending
- 2009-11-09 JP JP2009256398A patent/JP2010116397A/ja active Pending
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Legal Events
Date | Code | Title | Description |
---|---|---|---|
MM4A | Patent lapsed due to non-payment of maintenance fees |
Effective date: 20120504 |