DK1499623T3 - Fremgangsmåde til fremstilling af 1,2,3,9-tetrahydro-9-methyl-3-[(2-methyl-1H-imidazol-1-yl)methyl]-4H-carbazol-4-on - Google Patents
Fremgangsmåde til fremstilling af 1,2,3,9-tetrahydro-9-methyl-3-[(2-methyl-1H-imidazol-1-yl)methyl]-4H-carbazol-4-onInfo
- Publication number
- DK1499623T3 DK1499623T3 DK03719968T DK03719968T DK1499623T3 DK 1499623 T3 DK1499623 T3 DK 1499623T3 DK 03719968 T DK03719968 T DK 03719968T DK 03719968 T DK03719968 T DK 03719968T DK 1499623 T3 DK1499623 T3 DK 1499623T3
- Authority
- DK
- Denmark
- Prior art keywords
- methyl
- carbazol
- imidazol
- tetrahydro
- preparation
- Prior art date
Links
- 238000000034 method Methods 0.000 title abstract 3
- FELGMEQIXOGIFQ-UHFFFAOYSA-N Ondansetron Chemical compound CC1=NC=CN1CC1C(=O)C(C=2C(=CC=CC=2)N2C)=C2CC1 FELGMEQIXOGIFQ-UHFFFAOYSA-N 0.000 title 1
- FELGMEQIXOGIFQ-CYBMUJFWSA-N (3r)-9-methyl-3-[(2-methylimidazol-1-yl)methyl]-2,3-dihydro-1h-carbazol-4-one Chemical compound CC1=NC=CN1C[C@@H]1C(=O)C(C=2C(=CC=CC=2)N2C)=C2CC1 FELGMEQIXOGIFQ-CYBMUJFWSA-N 0.000 abstract 3
- 229960005343 ondansetron Drugs 0.000 abstract 3
- 238000005891 transamination reaction Methods 0.000 abstract 2
- 238000006683 Mannich reaction Methods 0.000 abstract 1
- 238000004519 manufacturing process Methods 0.000 abstract 1
- 239000011541 reaction mixture Substances 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
- C07D403/06—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 only aliphatic carbon atoms
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P1/00—Drugs for disorders of the alimentary tract or the digestive system
- A61P1/08—Drugs for disorders of the alimentary tract or the digestive system for nausea, cinetosis or vertigo; Antiemetics
-
- 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
- C07D209/82—Carbazoles; Hydrogenated carbazoles
- C07D209/88—Carbazoles; Hydrogenated carbazoles 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 carbon atoms of the ring system
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D521/00—Heterocyclic compounds containing unspecified hetero rings
Landscapes
- Organic Chemistry (AREA)
- Chemical & Material Sciences (AREA)
- Health & Medical Sciences (AREA)
- Hospice & Palliative Care (AREA)
- Otolaryngology (AREA)
- Engineering & Computer Science (AREA)
- Chemical Kinetics & Catalysis (AREA)
- General Chemical & Material Sciences (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Medicinal Chemistry (AREA)
- Life Sciences & Earth Sciences (AREA)
- Pharmacology & Pharmacy (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Animal Behavior & Ethology (AREA)
- General Health & Medical Sciences (AREA)
- Public Health (AREA)
- Veterinary Medicine (AREA)
- Plural Heterocyclic Compounds (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Indole Compounds (AREA)
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US37632302P | 2002-04-29 | 2002-04-29 | |
| PCT/US2003/013221 WO2003093281A1 (en) | 2002-04-29 | 2003-04-29 | Process for preparing 1,2,3,9-tetrahydro-9-methyl-3-[(2-methyl-1h-imidazol-1-yl)methyl]-4h-carbazol-4-one |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| DK1499623T3 true DK1499623T3 (da) | 2007-10-08 |
Family
ID=29401332
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| DK03719968T DK1499623T3 (da) | 2002-04-29 | 2003-04-29 | Fremgangsmåde til fremstilling af 1,2,3,9-tetrahydro-9-methyl-3-[(2-methyl-1H-imidazol-1-yl)methyl]-4H-carbazol-4-on |
Country Status (19)
| Country | Link |
|---|---|
| US (2) | US7098345B2 (da) |
| EP (1) | EP1499623B1 (da) |
| JP (1) | JP2005529142A (da) |
| KR (1) | KR20040104654A (da) |
| CN (1) | CN1665823A (da) |
| AT (1) | ATE364611T1 (da) |
| AU (1) | AU2003223764A1 (da) |
| CA (1) | CA2483566A1 (da) |
| DE (1) | DE60314400T2 (da) |
| DK (1) | DK1499623T3 (da) |
| ES (1) | ES2288606T3 (da) |
| HR (1) | HRP20041070A2 (da) |
| IL (1) | IL164904A0 (da) |
| MX (1) | MXPA04010846A (da) |
| NO (1) | NO20045192L (da) |
| PL (1) | PL373191A1 (da) |
| PT (1) | PT1499623E (da) |
| WO (1) | WO2003093281A1 (da) |
| ZA (1) | ZA200408934B (da) |
Families Citing this family (5)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| AU2002230935A1 (en) * | 2000-10-30 | 2002-05-15 | Teva Pharmaceutical Industries Ltd. | Novel crystal and solvate forms of ondansetron hydrochloride and processes for their preparation |
| US20050131045A1 (en) * | 2002-04-30 | 2005-06-16 | Judith Aronhime | Novel crystal forms of ondansetron, processes for their preparation, pharmaceutical, compositions containing the novel forms and methods for treating nausea using them |
| KR20040104677A (ko) * | 2002-04-30 | 2004-12-10 | 비오갈 기오기스제르갸르 알티. | 신규의 온단세트론 결정 형태, 그 제조 방법, 그 신규의결정 형태를 함유하는 약학 조성물 및 이들을 이용한구역질 치료 방법 |
| US7696356B2 (en) * | 2004-08-17 | 2010-04-13 | Taro Pharmaceutical Industries Limited | Process for preparing 1,2,3,9-tetrahydro-9-methyl-3-methylene-4H-carbazol-4-one and ondansetron therefrom |
| WO2006046253A1 (en) * | 2004-10-26 | 2006-05-04 | Ipca Laboratories Limited | A one-pot process for the preparation of antiemetic agent, 1,2,3,9-tetrahydro-9-methyl-3[(2-methyl)-1h-imidazole-1-yl)methyl]-4h-carbazol-4-o |
Family Cites Families (22)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| SE460359B (sv) | 1984-01-25 | 1989-10-02 | Glaxo Group Ltd | 3-imidazolylmetyltetrahydrokarbazoloner, foerfarande foer framstaellning av dessa och en farmaceutisk komposition |
| US4695578A (en) * | 1984-01-25 | 1987-09-22 | Glaxo Group Limited | 1,2,3,9-tetrahydro-3-imidazol-1-ylmethyl-4H-carbazol-4-ones, composition containing them, and method of using them to treat neuronal 5HT function disturbances |
| EP0201165B1 (en) | 1985-03-14 | 1994-07-20 | Beecham Group Plc | Medicaments for the treatment of emesis |
| GB8518745D0 (en) | 1985-07-24 | 1985-08-29 | Glaxo Group Ltd | Heterocyclic compounds |
| GB8518742D0 (en) | 1985-07-24 | 1985-08-29 | Glaxo Group Ltd | Process |
| GB8518741D0 (en) | 1985-07-24 | 1985-08-29 | Glaxo Group Ltd | Process |
| GB8518743D0 (en) * | 1985-07-24 | 1985-08-29 | Glaxo Group Ltd | Heterocyclic compounds |
| US4859662A (en) | 1986-11-28 | 1989-08-22 | Glaxo Group Limited | Tetrahydro-imidazolylmethylcarbazolones and analogs thereof for treating 5-HT function disturbances |
| GB8630071D0 (en) | 1986-12-17 | 1987-01-28 | Glaxo Group Ltd | Medicaments |
| GB8816187D0 (en) * | 1988-07-07 | 1988-08-10 | Glaxo Group Ltd | Medicaments |
| US5344658A (en) | 1989-06-28 | 1994-09-06 | Glaxo Group Limited | Process and composition using ondansetron |
| GB8914804D0 (en) | 1989-06-28 | 1989-08-16 | Glaxo Group Ltd | Process |
| JPH06508836A (ja) | 1991-06-26 | 1994-10-06 | セプラコア,インコーポレーテッド | 光学的に純粋なr(+)オンダンセトロンを使用する嘔吐、吐き気および他の障害の治療のための方法および組成物 |
| CA2106642C (en) | 1992-10-14 | 2005-08-16 | Peter Bod | Carbazolone derivatives and process for preparing the same |
| GB9423588D0 (en) | 1994-11-22 | 1995-01-11 | Glaxo Wellcome Inc | Compositions |
| GB9423511D0 (en) | 1994-11-22 | 1995-01-11 | Glaxo Wellcome Inc | Compositions |
| CN1045437C (zh) | 1994-12-29 | 1999-10-06 | 中国科学院上海有机化学研究所 | 恩丹西酮及其生理盐的合成 |
| AU2002230935A1 (en) | 2000-10-30 | 2002-05-15 | Teva Pharmaceutical Industries Ltd. | Novel crystal and solvate forms of ondansetron hydrochloride and processes for their preparation |
| EP1207160A1 (en) | 2000-11-20 | 2002-05-22 | Hanmi Pharm. Co., Ltd. | Process for the preparation of 1,2,3,9-tetrahydro-9-methyl-3-((2-methyl-1H-imidazol-1-yl)-methyl)-4H-carbazol-4-one |
| SK9892003A3 (en) | 2001-01-11 | 2004-05-04 | Teva Pharma | An improved process for preparing pure ondansetron hydrochloride dihydrate |
| WO2003090730A1 (en) | 2002-04-25 | 2003-11-06 | Generics [Uk] Limited | Novel crystalline forms of celecoxib and other compounds |
| KR20040104677A (ko) | 2002-04-30 | 2004-12-10 | 비오갈 기오기스제르갸르 알티. | 신규의 온단세트론 결정 형태, 그 제조 방법, 그 신규의결정 형태를 함유하는 약학 조성물 및 이들을 이용한구역질 치료 방법 |
-
2003
- 2003-04-29 DK DK03719968T patent/DK1499623T3/da active
- 2003-04-29 CN CN038154684A patent/CN1665823A/zh active Pending
- 2003-04-29 DE DE60314400T patent/DE60314400T2/de not_active Expired - Fee Related
- 2003-04-29 MX MXPA04010846A patent/MXPA04010846A/es unknown
- 2003-04-29 CA CA002483566A patent/CA2483566A1/en not_active Abandoned
- 2003-04-29 KR KR10-2004-7017346A patent/KR20040104654A/ko not_active Ceased
- 2003-04-29 AU AU2003223764A patent/AU2003223764A1/en not_active Abandoned
- 2003-04-29 HR HR20041070A patent/HRP20041070A2/hr not_active Application Discontinuation
- 2003-04-29 WO PCT/US2003/013221 patent/WO2003093281A1/en not_active Ceased
- 2003-04-29 JP JP2004501420A patent/JP2005529142A/ja active Pending
- 2003-04-29 PT PT03719968T patent/PT1499623E/pt unknown
- 2003-04-29 PL PL03373191A patent/PL373191A1/xx not_active Application Discontinuation
- 2003-04-29 US US10/425,450 patent/US7098345B2/en not_active Expired - Fee Related
- 2003-04-29 EP EP03719968A patent/EP1499623B1/en not_active Expired - Lifetime
- 2003-04-29 AT AT03719968T patent/ATE364611T1/de not_active IP Right Cessation
- 2003-04-29 ES ES03719968T patent/ES2288606T3/es not_active Expired - Lifetime
-
2004
- 2004-10-28 IL IL16490404A patent/IL164904A0/xx unknown
- 2004-11-04 ZA ZA200408934A patent/ZA200408934B/xx unknown
- 2004-11-26 NO NO20045192A patent/NO20045192L/no not_active Application Discontinuation
-
2006
- 2006-07-07 US US11/482,486 patent/US20060252942A1/en not_active Abandoned
Also Published As
| Publication number | Publication date |
|---|---|
| EP1499623A1 (en) | 2005-01-26 |
| MXPA04010846A (es) | 2005-01-25 |
| US7098345B2 (en) | 2006-08-29 |
| AU2003223764A1 (en) | 2003-11-17 |
| ZA200408934B (en) | 2006-07-26 |
| IL164904A0 (en) | 2005-12-18 |
| US20060252942A1 (en) | 2006-11-09 |
| DE60314400D1 (de) | 2007-07-26 |
| ATE364611T1 (de) | 2007-07-15 |
| DE60314400T2 (de) | 2008-02-07 |
| CN1665823A (zh) | 2005-09-07 |
| ES2288606T3 (es) | 2008-01-16 |
| JP2005529142A (ja) | 2005-09-29 |
| CA2483566A1 (en) | 2003-11-13 |
| KR20040104654A (ko) | 2004-12-10 |
| WO2003093281A1 (en) | 2003-11-13 |
| EP1499623B1 (en) | 2007-06-13 |
| HRP20041070A2 (en) | 2005-02-28 |
| PT1499623E (pt) | 2007-08-10 |
| NO20045192L (no) | 2005-01-28 |
| PL373191A1 (en) | 2005-08-22 |
| US20050020655A1 (en) | 2005-01-27 |
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| MX2021000795A (es) | Compuestos heterociclicos para inhibir la actividad de shp2. | |
| TW200626580A (en) | Synthesis of (5-bromo-4-methyl-pyridin-3-ylmethyl)-ethyl-carbamic acid tert-butyl ester | |
| NO20071629L (no) | Fremgangsmate for fremstilling av 2,7-oktadienylderivater | |
| MX2023002890A (es) | Procesos e intermedios para la preparacion de (s)-5-amino-3-(4-((5-fluoro-2-metoxibenzamido)metil)fenil)-1-(1,1 ,1-trifluoropropan-2-il)-1h-pirazol-4-carboxamida. | |
| ZA202403308B (en) | An efficient new process for synthesis of 2-amino-5-chloro-n-,3-dimethylbenzamide | |
| ZA202204277B (en) | Methods for the preparation of 5-bromo-2-(3-chloro-pyridin-2-yl)-2h-pyrazole-3-carboxylic acid | |
| NO20063132L (no) | Naftyridinderivater og deres anvendelse som modulatorer av muskarinreceptorer | |
| MXPA05013652A (es) | Modulador del receptor canabinoide. | |
| DK1499623T3 (da) | Fremgangsmåde til fremstilling af 1,2,3,9-tetrahydro-9-methyl-3-[(2-methyl-1H-imidazol-1-yl)methyl]-4H-carbazol-4-on | |
| WO2008021491A3 (en) | Method for synthesis of 8-alkoxy-9h-isothiazolo[5,4-b]quinoline-3,4-diones | |
| DK0595111T3 (da) | Carbazolonderivater og fremgangsmåde til deres fremstilling | |
| WO2004026267A3 (en) | Tri(alkylcarboxylato) gallium (iii) products and pharmaceutical compositions containing them | |
| NO20060417L (no) | Fremgangsmate til fremstilling av 1-okten fra krakk-C4 | |
| WO2004111047A3 (en) | Cycloalkanepyrrolopyridines as dp receptor antagonists | |
| IL185329A0 (en) | Conversion of 2-pyrazolines to pyrazoles using bromine | |
| DK1102765T3 (da) | Fremgangsmåde til syntese af (1H)-benzo[c]quinolizin-3-on-derivater | |
| MX2022006142A (es) | Proceso para la sintesis de (3-cloro-2-piridil)hidrazina. | |
| TW200510323A (en) | Process for the preparation of nonpeptide substituted spirobenzoazepine derivatives | |
| DK1389188T3 (da) | Fremgangsmåde til fremstilling af biperiden II | |
| WO2005047215A3 (en) | Processes for preparing bicyclo [3.1.0] hexane derivatives, and intermediates thereto | |
| TW200626555A (en) | A process for the preparation of 1, 3, 5-trisubstituted pyrazoles via [3+2] cycloaddition | |
| IL173582A0 (en) | A process for the preparation of phenyltetrazole derivatives | |
| WO2019097306A3 (en) | Synthesis of 5-amino-1-(2,6-dichloro-4-trifluoromethyl-phenyl)-4-ethylsulfanyl-1h-pyrazole-3-carbonitrile and related compounds | |
| ZA202307488B (en) | Methods for the preparation of 5-bromo-2-(3-chloro-pyridin-2-yl)-2h-pyrazole-3-carboxylic acid | |
| MA56071A (fr) | Procédés de préparation de 3-bromo-1-(3-chloropyridine-2-yl)-1h-pyrazole-5-carboxylate d'éthyle |