PE20060307A1 - Proceso de amonolisis enzimatica para preparacion de compuestos intermediarios para inhibidores de dipeptidilo peptidasa iv - Google Patents
Proceso de amonolisis enzimatica para preparacion de compuestos intermediarios para inhibidores de dipeptidilo peptidasa ivInfo
- Publication number
- PE20060307A1 PE20060307A1 PE2005000497A PE2005000497A PE20060307A1 PE 20060307 A1 PE20060307 A1 PE 20060307A1 PE 2005000497 A PE2005000497 A PE 2005000497A PE 2005000497 A PE2005000497 A PE 2005000497A PE 20060307 A1 PE20060307 A1 PE 20060307A1
- Authority
- PE
- Peru
- Prior art keywords
- preparation
- intermediary
- amonolysis
- dipeptidyl peptidase
- ester
- Prior art date
Links
- 150000001875 compounds Chemical class 0.000 title abstract 3
- 238000000034 method Methods 0.000 title abstract 2
- 102000016622 Dipeptidyl Peptidase 4 Human genes 0.000 title 1
- 102000004190 Enzymes Human genes 0.000 title 1
- 108090000790 Enzymes Proteins 0.000 title 1
- 101000930822 Giardia intestinalis Dipeptidyl-peptidase 4 Proteins 0.000 title 1
- 239000003112 inhibitor Substances 0.000 title 1
- QGZKDVFQNNGYKY-UHFFFAOYSA-N Ammonia Chemical compound N QGZKDVFQNNGYKY-UHFFFAOYSA-N 0.000 abstract 4
- -1 1,1-DIMETHYL ETHYL Chemical class 0.000 abstract 3
- 239000002253 acid Substances 0.000 abstract 3
- 229910021529 ammonia Inorganic materials 0.000 abstract 2
- 150000002148 esters Chemical class 0.000 abstract 2
- 108010031797 Candida antarctica lipase B Proteins 0.000 abstract 1
- 229940124213 Dipeptidyl peptidase 4 (DPP IV) inhibitor Drugs 0.000 abstract 1
- 108090000604 Hydrolases Proteins 0.000 abstract 1
- 102000004157 Hydrolases Human genes 0.000 abstract 1
- BVCZEBOGSOYJJT-UHFFFAOYSA-N ammonium carbamate Chemical compound [NH4+].NC([O-])=O BVCZEBOGSOYJJT-UHFFFAOYSA-N 0.000 abstract 1
- KXDHJXZQYSOELW-UHFFFAOYSA-N carbonic acid monoamide Natural products NC(O)=O KXDHJXZQYSOELW-UHFFFAOYSA-N 0.000 abstract 1
- 206010012601 diabetes mellitus Diseases 0.000 abstract 1
- 239000003603 dipeptidyl peptidase IV inhibitor Substances 0.000 abstract 1
- 230000002255 enzymatic effect Effects 0.000 abstract 1
- WCYWZMWISLQXQU-UHFFFAOYSA-N methyl Chemical class [CH3] WCYWZMWISLQXQU-UHFFFAOYSA-N 0.000 abstract 1
- 244000005700 microbiome Species 0.000 abstract 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D207/00—Heterocyclic compounds containing five-membered rings not condensed with other rings, with one nitrogen atom as the only ring hetero atom
- C07D207/02—Heterocyclic compounds containing five-membered rings not condensed with other rings, with one nitrogen atom as the only ring hetero atom with only hydrogen or carbon atoms directly attached to the ring nitrogen atom
- C07D207/18—Heterocyclic compounds containing five-membered rings not condensed with other rings, with one nitrogen atom as the only ring hetero atom with only hydrogen or carbon atoms directly attached to the ring nitrogen atom having one double bond between ring members or between a ring member and a non-ring member
- C07D207/22—Heterocyclic compounds containing five-membered rings not condensed with other rings, with one nitrogen atom as the only ring hetero atom with only hydrogen or carbon atoms directly attached to the ring nitrogen atom having one double bond between ring members or between a ring member and a non-ring member 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
-
- 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
- C07D209/02—Heterocyclic compounds containing five-membered rings, condensed with other rings, with one nitrogen atom as the only ring hetero atom condensed with one carbocyclic ring
- C07D209/52—Heterocyclic compounds containing five-membered rings, condensed with other rings, with one nitrogen atom as the only ring hetero atom condensed with one carbocyclic ring condensed with a ring other than six-membered
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07K—PEPTIDES
- C07K5/00—Peptides containing up to four amino acids in a fully defined sequence; Derivatives thereof
- C07K5/04—Peptides containing up to four amino acids in a fully defined sequence; Derivatives thereof containing only normal peptide links
- C07K5/06—Dipeptides
- C07K5/06008—Dipeptides with the first amino acid being neutral
- C07K5/06078—Dipeptides with the first amino acid being neutral and aromatic or cycloaliphatic
-
- 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
- C12P13/04—Alpha- or beta- amino 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
- 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
-
- 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
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Life Sciences & Earth Sciences (AREA)
- Zoology (AREA)
- Wood Science & Technology (AREA)
- Engineering & Computer Science (AREA)
- Health & Medical Sciences (AREA)
- Biochemistry (AREA)
- General Health & Medical Sciences (AREA)
- Genetics & Genomics (AREA)
- General Engineering & Computer Science (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Biotechnology (AREA)
- Chemical Kinetics & Catalysis (AREA)
- General Chemical & Material Sciences (AREA)
- Microbiology (AREA)
- Biophysics (AREA)
- Proteomics, Peptides & Aminoacids (AREA)
- Molecular Biology (AREA)
- Medicinal Chemistry (AREA)
- Preparation Of Compounds By Using Micro-Organisms (AREA)
- Nitrogen Condensed Heterocyclic Rings (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
Abstract
SE REFIERE A UN PROCESO DE PREPARACION DE UN COMPUESTO INTERMEDIARIO (A) ESTER 1-(1,1-DIMETIL ETILICO) DEL ACIDO (5S)-5-AMINOCARBONIL-4,5-DIHIDRO-1H-PIRROLO-1-CARBOXILICO TAMBIEN REFERIDO COMO ESTER 1-(1,1-DIMETIL ETILICO) DEL ACIDO (2S)-2-AMINOCARBONIL-2,3-DIHIDRO-1H-PIRROLO-1-CARBOXILICO, QUE CONSISTE EN SOMETER UN COMPUESTO (B) ESTER 1-(1,1-DIMETILETIL)-5-ETILICO O METILICO DEL ACIDO (5S)-4,5-DIHIDRO-1H-PIRROLO-1,5-CARBOXILICO A UNA AMONOLISIS ENZIMATICA EN LA PRESENCIA DE UNA FUENTE DE AMONIACO COMO CARBAMATO DE AMONIO, GAS DE AMONIACO, ENTRE OTROS PARA PRODUCIR EL INTERMEDIARIO (A), EMPLEANDOSE LA ENZIMA HIDROLASA LA CUAL ES DERIVADA DEL MICROORGANISMO CANDIDA ANTARCTICA LIPASA-B. ESTE INTERMEDIARIO (A) ES UTIL EN LA PREPARACION DE UN INHIBIDOR DE DIPEPTIDILO PEPTIDASA IV (1S,3S,5S)-2-[(2S)-2-AMINO-2-(3-HIDROXITRICICLO[3.3.1.1(3.7)]-DEC-1-IL)-1-OXOETIL]-2-AZABICICLO{3.1.0}HEXANO-3-CARBONITRILO, EL CUAL ES UTIL PARA EL TRATAMIENTO DE DIABETES
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US56809704P | 2004-05-04 | 2004-05-04 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| PE20060307A1 true PE20060307A1 (es) | 2006-04-20 |
Family
ID=35320243
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| PE2005000497A PE20060307A1 (es) | 2004-05-04 | 2005-05-04 | Proceso de amonolisis enzimatica para preparacion de compuestos intermediarios para inhibidores de dipeptidilo peptidasa iv |
Country Status (5)
| Country | Link |
|---|---|
| US (2) | US7223573B2 (es) |
| AR (1) | AR048651A1 (es) |
| PE (1) | PE20060307A1 (es) |
| TW (1) | TW200536827A (es) |
| WO (1) | WO2005108594A1 (es) |
Families Citing this family (12)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US7420079B2 (en) * | 2002-12-09 | 2008-09-02 | Bristol-Myers Squibb Company | Methods and compounds for producing dipeptidyl peptidase IV inhibitors and intermediates thereof |
| US7741082B2 (en) | 2004-04-14 | 2010-06-22 | Bristol-Myers Squibb Company | Process for preparing dipeptidyl peptidase IV inhibitors and intermediates therefor |
| KR20110135411A (ko) * | 2009-03-27 | 2011-12-16 | 브리스톨-마이어스 스큅 컴퍼니 | Dpp-iv 억제제로 주요 유해 심장혈관 이벤트를 예방하는 방법 |
| EA201291169A1 (ru) | 2010-05-05 | 2013-04-30 | Ассия Кемикал Индастриз Лтд. | Промежуточные соединения саксаглиптина, полиморфы саксаглиптина и способы их получения |
| WO2012047871A1 (en) | 2010-10-04 | 2012-04-12 | Assia Chemical Industries Ltd | Polymorphs of saxagliptin hydrochloride and processes for preparing them |
| CN104098481B (zh) * | 2013-04-10 | 2016-05-11 | 浙江九洲药物科技有限公司 | 一种沙格列汀中间体的制备方法 |
| CN103951588B (zh) * | 2014-04-30 | 2016-10-05 | 淮海工学院 | 一种合成沙格列汀中间体n-叔丁氧羰基-3-羟基-1-金刚烷基-d-甘氨酸的方法 |
| CN105315189A (zh) * | 2014-05-29 | 2016-02-10 | 上海医药工业研究院 | 一种制备(5s)-5-氨基羰基-4,5-二氢-1h-吡咯-1-羧酸-1(1,1-二甲基乙基)酯的方法 |
| WO2016144862A1 (en) | 2015-03-09 | 2016-09-15 | Intekrin Therapeutics, Inc. | Methods for the treatment of nonalcoholic fatty liver disease and/or lipodystrophy |
| KR20200036808A (ko) | 2017-04-03 | 2020-04-07 | 코히러스 바이오사이언시스, 인크. | 진행성 핵상 마비 치료를 위한 PPARγ 작용제 |
| KR102796813B1 (ko) | 2020-06-24 | 2025-04-16 | 삼성전자주식회사 | 반도체 패키지 및 반도체 패키지의 제조 방법 |
| CN114369061B (zh) * | 2022-01-28 | 2024-05-03 | 济南同路医药科技发展有限公司 | 一种氯硝西泮有关物质b的制备方法 |
Family Cites Families (5)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| IL120873A0 (en) | 1996-05-24 | 1997-09-30 | Tanabe Seiyaku Co | Process for preparing optically active 2-halogen-3-hydroxypropionic acid ester |
| US6068991A (en) * | 1997-12-16 | 2000-05-30 | Bristol-Myers Squibb Company | High expression Escherichia coli expression vector |
| JP2002520065A (ja) | 1998-07-15 | 2002-07-09 | ブリストル−マイヤーズ スクイブ カンパニー | ケトンの立体選択的還元的アミノ化 |
| US6395767B2 (en) * | 2000-03-10 | 2002-05-28 | Bristol-Myers Squibb Company | Cyclopropyl-fused pyrrolidine-based inhibitors of dipeptidyl peptidase IV and method |
| US7420079B2 (en) | 2002-12-09 | 2008-09-02 | Bristol-Myers Squibb Company | Methods and compounds for producing dipeptidyl peptidase IV inhibitors and intermediates thereof |
-
2005
- 2005-04-28 TW TW094113728A patent/TW200536827A/zh unknown
- 2005-05-02 US US11/119,552 patent/US7223573B2/en not_active Expired - Lifetime
- 2005-05-03 WO PCT/US2005/015199 patent/WO2005108594A1/en not_active Ceased
- 2005-05-03 AR ARP050101778A patent/AR048651A1/es not_active Application Discontinuation
- 2005-05-04 PE PE2005000497A patent/PE20060307A1/es not_active Application Discontinuation
-
2007
- 2007-04-18 US US11/736,786 patent/US7611880B2/en active Active
Also Published As
| Publication number | Publication date |
|---|---|
| US7611880B2 (en) | 2009-11-03 |
| AR048651A1 (es) | 2006-05-10 |
| US20050256019A1 (en) | 2005-11-17 |
| US20070207527A1 (en) | 2007-09-06 |
| TW200536827A (en) | 2005-11-16 |
| WO2005108594A1 (en) | 2005-11-17 |
| US7223573B2 (en) | 2007-05-29 |
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Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| FD | Application declared void or lapsed |