NO20073984L - Preparation of tetrazole derivatives - Google Patents
Preparation of tetrazole derivativesInfo
- Publication number
- NO20073984L NO20073984L NO20073984A NO20073984A NO20073984L NO 20073984 L NO20073984 L NO 20073984L NO 20073984 A NO20073984 A NO 20073984A NO 20073984 A NO20073984 A NO 20073984A NO 20073984 L NO20073984 L NO 20073984L
- Authority
- NO
- Norway
- Prior art keywords
- preparation
- irbesartan
- pharmaceutically acceptable
- tetrazole derivatives
- tetrazole
- Prior art date
Links
- 238000002360 preparation method Methods 0.000 title abstract 2
- 150000003536 tetrazoles Chemical class 0.000 title 1
- 150000003839 salts Chemical class 0.000 abstract 3
- 239000002947 C09CA04 - Irbesartan Substances 0.000 abstract 2
- YCPOHTHPUREGFM-UHFFFAOYSA-N irbesartan Chemical compound O=C1N(CC=2C=CC(=CC=2)C=2C(=CC=CC=2)C=2[N]N=NN=2)C(CCCC)=NC21CCCC2 YCPOHTHPUREGFM-UHFFFAOYSA-N 0.000 abstract 2
- 229960002198 irbesartan Drugs 0.000 abstract 2
- NDTNRUYCXAKMPU-UHFFFAOYSA-N 2-butyl-3-[[4-[2-(2-trityltetrazol-5-yl)phenyl]phenyl]methyl]-1,3-diazaspiro[4.4]non-1-en-4-one Chemical compound O=C1N(CC=2C=CC(=CC=2)C=2C(=CC=CC=2)C2=NN(N=N2)C(C=2C=CC=CC=2)(C=2C=CC=CC=2)C=2C=CC=CC=2)C(CCCC)=NC21CCCC2 NDTNRUYCXAKMPU-UHFFFAOYSA-N 0.000 abstract 1
- 230000015572 biosynthetic process Effects 0.000 abstract 1
- 238000006243 chemical reaction Methods 0.000 abstract 1
- 238000002955 isolation Methods 0.000 abstract 1
- 238000000034 method Methods 0.000 abstract 1
- 239000003960 organic solvent Substances 0.000 abstract 1
- 239000003444 phase transfer catalyst Substances 0.000 abstract 1
- 125000006239 protecting group Chemical group 0.000 abstract 1
- 238000003786 synthesis reaction Methods 0.000 abstract 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D403/00—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00
- C07D403/02—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00 containing two hetero rings
- C07D403/10—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00 containing two hetero rings linked by a carbon chain containing aromatic rings
-
- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y02—TECHNOLOGIES OR APPLICATIONS FOR MITIGATION OR ADAPTATION AGAINST CLIMATE CHANGE
- Y02P—CLIMATE CHANGE MITIGATION TECHNOLOGIES IN THE PRODUCTION OR PROCESSING OF GOODS
- Y02P20/00—Technologies relating to chemical industry
- Y02P20/50—Improvements relating to the production of bulk chemicals
- Y02P20/55—Design of synthesis routes, e.g. reducing the use of auxiliary or protecting groups
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Plural Heterocyclic Compounds (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Low-Molecular Organic Synthesis Reactions Using Catalysts (AREA)
Abstract
Den foreliggende oppfinnelsen angår en fremgangsmåte for fremstillingen av irbesartan eller dets farmasøytisk akseptable salter, som omfatter en syntese av tritylirbesartan ved en reaksjon mellom 5-(4-brommetyl)bifenyl-2-yl)-1-(trifenylmetyl)tetrazol og 2-n-butyl-4-syklopentan-2-imidazolin-5-on eller et salt av disse, i et organisk løsemiddel i nærvær av en faseoverføringskatalysator og en base, en fjerning av den beskyttende gruppen og en isolering av irbesartan eller dets farmasøytisk akseptable salt.The present invention relates to a process for the preparation of irbesartan or its pharmaceutically acceptable salts, which comprises a synthesis of tritylirbesartan by a reaction of 5- (4-bromomethyl) biphenyl-2-yl) -1- (triphenylmethyl) tetrazole and 2-n. -butyl-4-cyclopentan-2-imidazolin-5-one or a salt thereof, in an organic solvent in the presence of a phase transfer catalyst and a base, a removal of the protecting group and an isolation of irbesartan or its pharmaceutically acceptable salt.
Applications Claiming Priority (3)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| SI200500004A SI21964A (en) | 2005-01-05 | 2005-01-05 | Preparation of tetrazole derivative |
| SI200500132A SI21965A (en) | 2005-01-05 | 2005-05-05 | Preparation of tetrazole derivative |
| PCT/SI2006/000001 WO2006073376A2 (en) | 2005-01-05 | 2006-01-04 | Preparation of irbesartan |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| NO20073984L true NO20073984L (en) | 2007-10-05 |
Family
ID=36129763
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| NO20073984A NO20073984L (en) | 2005-01-05 | 2007-07-31 | Preparation of tetrazole derivatives |
Country Status (5)
| Country | Link |
|---|---|
| EP (1) | EP2049527A2 (en) |
| EA (1) | EA012852B1 (en) |
| NO (1) | NO20073984L (en) |
| SI (1) | SI21965A (en) |
| WO (1) | WO2006073376A2 (en) |
Families Citing this family (5)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| EP1916246A3 (en) * | 2006-10-11 | 2008-06-18 | Cadila Pharmaceuticals Limited | An improved process for the preparation of olmesartan medoxomil |
| GB0700993D0 (en) * | 2007-01-18 | 2007-02-28 | Rainbow Engineering Services | Novel compounds |
| GB0700992D0 (en) * | 2007-01-18 | 2007-02-28 | Rainbow Engineering Services | Novel compounds |
| EP2194050A1 (en) | 2008-12-08 | 2010-06-09 | KRKA, tovarna zdravil, d.d., Novo mesto | A new process for the preparation of irbesartan |
| CN120392084B (en) * | 2025-04-10 | 2026-04-07 | 常州江苏大学工程技术研究院 | A pH-sensitive electrode comprising a wearable pH sensor for wound condition diagnosis and its application. |
Family Cites Families (4)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CN1668612A (en) * | 2002-07-16 | 2005-09-14 | 特瓦制药工业有限公司 | New Synthetic Method of Irbesartan |
| SI1509517T1 (en) * | 2003-01-16 | 2008-10-31 | Teva Pharma | Novel synthesis of irbesartan |
| WO2004072064A1 (en) * | 2003-02-05 | 2004-08-26 | Teva Pharmaceutical Industries Ltd. | Synthesis of 2-butyl-3-(2'-(1-trityl-1h-tetrazol-5-yl)biphenyl-4-yl)-1,3-diazaspirol[4,4]-non-ene-4-one |
| SI21849A (en) * | 2004-07-29 | 2006-02-28 | Krka, Tovarna Zdravil, D.D., Novo Mesto | Preparation of hydrochloride salts of tetrazole derivative |
-
2005
- 2005-05-05 SI SI200500132A patent/SI21965A/en not_active IP Right Cessation
-
2006
- 2006-01-04 EP EP06700020A patent/EP2049527A2/en not_active Withdrawn
- 2006-01-04 EA EA200701433A patent/EA012852B1/en not_active IP Right Cessation
- 2006-01-04 WO PCT/SI2006/000001 patent/WO2006073376A2/en not_active Ceased
-
2007
- 2007-07-31 NO NO20073984A patent/NO20073984L/en not_active Application Discontinuation
Also Published As
| Publication number | Publication date |
|---|---|
| EP2049527A2 (en) | 2009-04-22 |
| EA200701433A1 (en) | 2008-02-28 |
| WO2006073376A3 (en) | 2006-09-21 |
| SI21965A (en) | 2006-08-31 |
| EA012852B1 (en) | 2009-12-30 |
| WO2006073376A2 (en) | 2006-07-13 |
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| NO20090295L (en) | Substituted heteroaryl derivatives | |
| JO2758B1 (en) | Process for the synthesis of organic compounds | |
| WO2009016460A8 (en) | Pyrazole compounds and their use as raf inhibitors | |
| WO2008084223A3 (en) | Chemical compounds 637: pyridopyrimidinediones as pde4 inhibitors | |
| MX2009008264A (en) | Heterocyclic spiro-compounds. | |
| WO2009016462A3 (en) | Substituted bicyclolactam compounds | |
| NO20090173L (en) | Condensed spiroketal derivative and its use as a drug for treating diabetes | |
| ATE555105T1 (en) | HETEROCYCLIC FXR BINDING COMPOUNDS | |
| NO20071242L (en) | Triazole pyridinylsulfanyl derivatives as P38-MAP kinase inhibitors | |
| BRPI0615705A2 (en) | process for preparing a compound and compound | |
| NO20071619L (en) | Process for the preparation of indazole compound | |
| NO20073984L (en) | Preparation of tetrazole derivatives | |
| WO2007065942A3 (en) | Bis-heterocyclic imidazolyl compounds | |
| TW200716105A (en) | Imidazole compounds | |
| WO2006128852A3 (en) | Heterocyclic spiro-compounds as aldosterone synthase inhibitors | |
| NO20083708L (en) | 4-Phenyl-thiazole-5-carboxylic acid and 4-phenyl-thiazole-5-carboxylmides as PLK1 inhibitors | |
| UA100125C2 (en) | Method for isolation and purification of montelukast | |
| CL2009001414A1 (en) | Process for the synthesis of 7,8-dimethoxy-1,3-dihydro-2h-3-benzazepin-2-one without isolation of intermediate compounds; useful for the synthesis of ivabradine. | |
| NO20080750L (en) | (Indol-3-YL) heterocycle derivatives as agonists of cannabinoid CB1 receptor | |
| CR11824A (en) | HETEROCYCLIC DERIVATIVES OF UREA AND ITS EMPLOYMENT METHODS | |
| NO20060729L (en) | Process for the preparation of tetrazole derivatives from organic boron and aluminum azides | |
| UA94603C2 (en) | Tetrahydronaphthaline derivatives, methods for the production and use thereof as anti-inflammatory agents | |
| AU2012264476A8 (en) | Process for the preparation of paliperidone | |
| DE602004005488D1 (en) | PROCESS FOR THE PREPARATION OF CANDESARTAN CILEXETIL | |
| WO2009071691A3 (en) | Oxindole derivatives and the use thereof as a medication |
Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| FC2A | Withdrawal, rejection or dismissal of laid open patent application |