JP2006137778A5 - - Google Patents
Download PDFInfo
- Publication number
- JP2006137778A5 JP2006137778A5 JP2006033099A JP2006033099A JP2006137778A5 JP 2006137778 A5 JP2006137778 A5 JP 2006137778A5 JP 2006033099 A JP2006033099 A JP 2006033099A JP 2006033099 A JP2006033099 A JP 2006033099A JP 2006137778 A5 JP2006137778 A5 JP 2006137778A5
- Authority
- JP
- Japan
- Prior art keywords
- zolpidem hemitartrate
- acid
- zolpidem
- forming
- halide
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Pending
Links
- VXRDAMSNTXUHFX-CEAXSRTFSA-N zolpidem tartrate Chemical compound OC(=O)[C@H](O)[C@@H](O)C(O)=O.N1=C2C=CC(C)=CN2C(CC(=O)N(C)C)=C1C1=CC=C(C)C=C1.N1=C2C=CC(C)=CN2C(CC(=O)N(C)C)=C1C1=CC=C(C)C=C1 VXRDAMSNTXUHFX-CEAXSRTFSA-N 0.000 claims 16
- 238000000034 method Methods 0.000 claims 10
- YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 claims 8
- 239000002253 acid Substances 0.000 claims 6
- 238000000634 powder X-ray diffraction Methods 0.000 claims 6
- 150000004820 halides Chemical class 0.000 claims 5
- JHGHLTNIQXXXNV-UHFFFAOYSA-N 2-[6-methyl-2-(4-methylphenyl)imidazo[1,2-a]pyridin-3-yl]acetic acid Chemical compound C1=CC(C)=CC=C1C1=C(CC(O)=O)N2C=C(C)C=CC2=N1 JHGHLTNIQXXXNV-UHFFFAOYSA-N 0.000 claims 4
- KFZMGEQAYNKOFK-UHFFFAOYSA-N Isopropanol Chemical compound CC(C)O KFZMGEQAYNKOFK-UHFFFAOYSA-N 0.000 claims 4
- LRHPLDYGYMQRHN-UHFFFAOYSA-N N-Butanol Chemical compound CCCCO LRHPLDYGYMQRHN-UHFFFAOYSA-N 0.000 claims 4
- ZAFYATHCZYHLPB-UHFFFAOYSA-N zolpidem Chemical compound N1=C2C=CC(C)=CN2C(CC(=O)N(C)C)=C1C1=CC=C(C)C=C1 ZAFYATHCZYHLPB-UHFFFAOYSA-N 0.000 claims 4
- 229960001475 zolpidem Drugs 0.000 claims 4
- ROSDSFDQCJNGOL-UHFFFAOYSA-N Dimethylamine Chemical compound CNC ROSDSFDQCJNGOL-UHFFFAOYSA-N 0.000 claims 2
- 239000002904 solvent Substances 0.000 claims 2
- -1 zolpidic acid halide Chemical class 0.000 claims 2
- VEXZGXHMUGYJMC-UHFFFAOYSA-M Chloride anion Chemical compound [Cl-] VEXZGXHMUGYJMC-UHFFFAOYSA-M 0.000 claims 1
- FEWJPZIEWOKRBE-JCYAYHJZSA-N Dextrotartaric acid Chemical compound OC(=O)[C@H](O)[C@@H](O)C(O)=O FEWJPZIEWOKRBE-JCYAYHJZSA-N 0.000 claims 1
- 235000011002 L(+)-tartaric acid Nutrition 0.000 claims 1
- 239000001358 L(+)-tartaric acid Substances 0.000 claims 1
- FEWJPZIEWOKRBE-LWMBPPNESA-N L-(+)-Tartaric acid Natural products OC(=O)[C@@H](O)[C@H](O)C(O)=O FEWJPZIEWOKRBE-LWMBPPNESA-N 0.000 claims 1
- FEWJPZIEWOKRBE-UHFFFAOYSA-N Tartaric acid Natural products [H+].[H+].[O-]C(=O)C(O)C(O)C([O-])=O FEWJPZIEWOKRBE-UHFFFAOYSA-N 0.000 claims 1
- 238000002441 X-ray diffraction Methods 0.000 claims 1
- 238000005660 chlorination reaction Methods 0.000 claims 1
- 238000010438 heat treatment Methods 0.000 claims 1
- RLOWWWKZYUNIDI-UHFFFAOYSA-N phosphinic chloride Chemical compound ClP=O RLOWWWKZYUNIDI-UHFFFAOYSA-N 0.000 claims 1
- 150000003839 salts Chemical class 0.000 claims 1
- 239000002002 slurry Substances 0.000 claims 1
- 230000002194 synthesizing effect Effects 0.000 claims 1
- 125000003944 tolyl group Chemical group 0.000 claims 1
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims 1
Applications Claiming Priority (3)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US19929800P | 2000-04-24 | 2000-04-24 | |
| US20602500P | 2000-05-22 | 2000-05-22 | |
| US22536400P | 2000-08-14 | 2000-08-14 |
Related Parent Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP2001577956A Division JP2003531173A (ja) | 2000-04-24 | 2001-04-24 | ゾルピデムヘミタートレイト |
Related Child Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP2006177160A Division JP2006249105A (ja) | 2000-04-24 | 2006-06-27 | ゾルピデムヘミタートレイト |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| JP2006137778A JP2006137778A (ja) | 2006-06-01 |
| JP2006137778A5 true JP2006137778A5 (enExample) | 2006-08-10 |
Family
ID=27394001
Family Applications (3)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP2001577956A Withdrawn JP2003531173A (ja) | 2000-04-24 | 2001-04-24 | ゾルピデムヘミタートレイト |
| JP2006033099A Pending JP2006137778A (ja) | 2000-04-24 | 2006-02-09 | ゾルピデムヘミタートレイト |
| JP2006177160A Pending JP2006249105A (ja) | 2000-04-24 | 2006-06-27 | ゾルピデムヘミタートレイト |
Family Applications Before (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP2001577956A Withdrawn JP2003531173A (ja) | 2000-04-24 | 2001-04-24 | ゾルピデムヘミタートレイト |
Family Applications After (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP2006177160A Pending JP2006249105A (ja) | 2000-04-24 | 2006-06-27 | ゾルピデムヘミタートレイト |
Country Status (21)
| Country | Link |
|---|---|
| US (8) | US20020077332A1 (enExample) |
| EP (1) | EP1292304B1 (enExample) |
| JP (3) | JP2003531173A (enExample) |
| KR (1) | KR20030069796A (enExample) |
| AT (4) | ATE348613T1 (enExample) |
| AU (2) | AU5721301A (enExample) |
| CA (1) | CA2406982A1 (enExample) |
| CZ (1) | CZ20023775A3 (enExample) |
| DE (7) | DE60122944T2 (enExample) |
| DK (1) | DK1292304T3 (enExample) |
| ES (4) | ES2277301T3 (enExample) |
| HR (1) | HRP20020909A2 (enExample) |
| HU (1) | HUP0300701A2 (enExample) |
| IL (1) | IL152411A0 (enExample) |
| NZ (1) | NZ522015A (enExample) |
| PL (1) | PL358548A1 (enExample) |
| PT (3) | PT1475093E (enExample) |
| SE (1) | SE5292304T3 (enExample) |
| SK (1) | SK16372002A3 (enExample) |
| WO (1) | WO2001080857A1 (enExample) |
| YU (1) | YU79402A (enExample) |
Families Citing this family (27)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| AU2001284322A1 (en) | 2000-08-29 | 2002-03-13 | Ranbaxy Laboratories Limited | Synthesis of n,n-dimethyl-3-(4-methyl) benzoyl propionamide, a key intermediate of zolpidem |
| US6869970B2 (en) | 2002-02-04 | 2005-03-22 | Novartis Ag | Crystalline salt forms of valsartan |
| US7385056B2 (en) | 2002-12-18 | 2008-06-10 | Mallinckrodt Inc. | Synthesis of heteroaryl acetamides |
| WO2004087703A1 (en) * | 2003-03-12 | 2004-10-14 | Sun Pharmaceutical Industries Limited | Process for the preparation of n,n,6-trimethyl-2-(4-methylphenyl)-imidazo[1,2-a]pyridine-3-acetamide |
| WO2005010002A1 (en) * | 2003-07-31 | 2005-02-03 | Ranbaxy Laboratories Limited | Process for the synthesis of zolpidem |
| US7658945B2 (en) * | 2004-02-17 | 2010-02-09 | Transcept Pharmaceuticals, Inc. | Compositions for delivering hypnotic agents across the oral mucosa and methods of use thereof |
| WO2006008636A2 (en) * | 2004-07-16 | 2006-01-26 | Ranbaxy Laboratories Limited | Processes for the preparation of zolpidem and its hemitartrate |
| NZ563979A (en) * | 2005-05-25 | 2011-02-25 | Transcept Pharmaceuticals Inc | Solid compositions and methods for treating middle-of-the night insomnia |
| US20070225322A1 (en) * | 2005-05-25 | 2007-09-27 | Transoral Pharmaceuticals, Inc. | Compositions and methods for treating middle-of-the night insomnia |
| US20070287740A1 (en) * | 2005-05-25 | 2007-12-13 | Transcept Pharmaceuticals, Inc. | Compositions and methods of treating middle-of-the night insomnia |
| AU2006283702A1 (en) * | 2005-08-19 | 2007-03-01 | Aventis Pharmaceuticals Inc. | Comination of a hypnotic agent and R(+)-alpha-(2,3-dimethoxy-phenyl)-1-(2-(4-fluorophenl)ethyl)-4-piperidinemethanol and therapeutic application thereof |
| CA2617980A1 (en) * | 2005-08-19 | 2007-03-01 | Aventis Pharmaceuticals Inc. | Combination of a hypnotic agent and substituted bis aryl and heteroaryl compound and therapeutic application thereof |
| WO2007040995A1 (en) * | 2005-10-03 | 2007-04-12 | Mallinckrodt Inc. | Process for preparing zolpidem hemitartrate and tartrate polymorphs |
| US20080200680A1 (en) * | 2005-10-17 | 2008-08-21 | Cheng Brian K | Polymorph Transformation of Zolpidem in Tablet Matrix |
| US20070098788A1 (en) * | 2005-10-28 | 2007-05-03 | Gore Subhash P | Non-benzodiazepine hypnotic compositions |
| CA2648036C (en) | 2006-03-31 | 2012-05-22 | Janssen Pharmaceutica N.V. | Benzoimidazol-2-yl pyrimidines and pyrazines as modulators of the histamine h4 receptor |
| US20080132535A1 (en) * | 2006-11-30 | 2008-06-05 | Transcept Pharmaceuticals, Inc. | Stabilized Zolpidem Pharmaceutical Compositions |
| US20080145425A1 (en) * | 2006-12-15 | 2008-06-19 | Pliva Research & Development Limited | Pharmaceutical composition of zolpidem |
| US9371311B2 (en) | 2008-06-30 | 2016-06-21 | Janssen Pharmaceutica Nv | Benzoimidazol-2-yl pyrimidine derivatives |
| EA020090B1 (ru) * | 2008-06-30 | 2014-08-29 | Янссен Фармацевтика Нв | Способ получения и рекристаллизации кристаллического гемитартрата бензоимидазол-2-илпиримидинового производного |
| CN102712629B (zh) | 2009-11-27 | 2016-10-12 | 基酶有限公司 | 作为葡糖神经酰胺合酶的抑制剂的无定型和结晶形式的Genz112638半酒石酸盐 |
| WO2011115069A1 (ja) * | 2010-03-19 | 2011-09-22 | 第一三共株式会社 | 結晶の網羅的探索 |
| ES2773543T3 (es) * | 2013-03-06 | 2020-07-13 | Janssen Pharmaceutica Nv | Benzoimidazol-2-ilpirimidinas moduladores del receptor de histamina H4 |
| CN116283958A (zh) * | 2021-12-03 | 2023-06-23 | 山东新时代药业有限公司 | 唑吡坦共晶体及其制备方法 |
| CN116283957A (zh) * | 2021-12-03 | 2023-06-23 | 山东新时代药业有限公司 | 唑吡坦水合物及其制备方法 |
| CN117907368A (zh) * | 2024-01-27 | 2024-04-19 | 鲁南贝特制药有限公司 | 一种酒石酸唑吡坦药用晶型d中晶型a、e的定量测定方法 |
| CN118750459B (zh) * | 2024-07-22 | 2025-04-01 | 常州市武进中医医院 | 一种酒石酸唑吡坦片及其制备方法 |
Family Cites Families (17)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US4151273A (en) * | 1974-10-31 | 1979-04-24 | The Regents Of The University Of California | Increasing the absorption rate of insoluble drugs |
| FR2408345A1 (fr) * | 1976-11-30 | 1979-06-08 | Besins Jean Louis | Nouvelle composition a action anti-conceptionnelle |
| US4302446A (en) * | 1979-10-02 | 1981-11-24 | Bristol-Myers Company | Pharmaceutical compositions |
| IT1130924B (it) * | 1980-03-06 | 1986-06-18 | Secifarma Spa | Procedimento per la preparazione di spironolattone micronizzato |
| DE3018940A1 (de) * | 1980-05-17 | 1981-11-26 | Hoechst Ag, 6000 Frankfurt | Verwendung eines vinylchlorid-pfropf-copolymerisates in der plastisolverarbeitung |
| FR2492382A1 (fr) * | 1980-10-22 | 1982-04-23 | Synthelabo | Derives d'imidazo (1,2-a) pyridine, leur preparation et leur application en therapeutique |
| FR2525601A1 (fr) * | 1982-04-21 | 1983-10-28 | Synthelabo | Derives d'imidazo(1,2-a)pyridines, leur preparation et leur application en therapeutique |
| US4675323A (en) * | 1985-08-06 | 1987-06-23 | Synthelabo | Imidazo(1,2-a)quinoline derivatives useful as anxiolytic agents |
| SE457326B (sv) * | 1986-02-14 | 1988-12-19 | Lejus Medical Ab | Foerfarande foer framstaellning av en snabbt soenderfallande kaerna innehaallande bl a mikrokristallin cellulosa |
| FR2600650B1 (fr) * | 1986-06-27 | 1988-09-09 | Synthelabo | Procede de preparation d'imidazopyridines et composes intermediaires |
| FR2606410B1 (fr) * | 1986-11-07 | 1989-02-24 | Synthelabo | Imidazopyridines, leur preparation et leur application en therapeutique |
| ES2026666T3 (es) * | 1987-03-27 | 1992-05-01 | Synthelabo | Procedimiento para preparar derivados de imidazopiridinas. |
| US5271944A (en) * | 1991-04-05 | 1993-12-21 | Biofor, Ltd. | Pharmacologically enhanced formulations |
| IT1276522B1 (it) * | 1995-04-07 | 1997-10-31 | Elena Benincasa | Uso dello zolpidem per il trattamento terapeudico di sindromi neuropsichiatriche associate a disfunsione e di circuiti neurali dei |
| AU3464200A (en) * | 1999-03-25 | 2000-10-16 | Synthon B.V. | Zolpidem salts |
| SI1038875T1 (en) * | 1999-03-25 | 2003-12-31 | Synthon B.V. | Imidazopyridine derivatives and process for making them |
| WO2001042239A1 (en) * | 1999-12-13 | 2001-06-14 | Sumika Fine Chemicals Co., Ltd. | Process for the preparation of a pyridinemethanol compound |
-
2001
- 2001-04-24 ES ES05001922T patent/ES2277301T3/es not_active Expired - Lifetime
- 2001-04-24 AT AT05001922T patent/ATE348613T1/de not_active IP Right Cessation
- 2001-04-24 US US09/841,025 patent/US20020077332A1/en not_active Abandoned
- 2001-04-24 SK SK1637-2002A patent/SK16372002A3/sk not_active Application Discontinuation
- 2001-04-24 ES ES04010435T patent/ES2238941T3/es not_active Expired - Lifetime
- 2001-04-24 IL IL15241101A patent/IL152411A0/xx unknown
- 2001-04-24 PT PT04010651T patent/PT1475093E/pt unknown
- 2001-04-24 AT AT04010651T patent/ATE338550T1/de not_active IP Right Cessation
- 2001-04-24 DE DE60122944T patent/DE60122944T2/de not_active Expired - Fee Related
- 2001-04-24 CZ CZ20023775A patent/CZ20023775A3/cs unknown
- 2001-04-24 DE DE60114617T patent/DE60114617T2/de not_active Expired - Fee Related
- 2001-04-24 PT PT04010435T patent/PT1473036E/pt unknown
- 2001-04-24 DE DE60125429T patent/DE60125429T2/de not_active Expired - Fee Related
- 2001-04-24 NZ NZ522015A patent/NZ522015A/en unknown
- 2001-04-24 AT AT04010435T patent/ATE335481T1/de not_active IP Right Cessation
- 2001-04-24 PT PT05001922T patent/PT1541146E/pt unknown
- 2001-04-24 ES ES01930705T patent/ES2248321T3/es not_active Expired - Lifetime
- 2001-04-24 PL PL01358548A patent/PL358548A1/xx not_active Application Discontinuation
- 2001-04-24 YU YU79402A patent/YU79402A/sh unknown
- 2001-04-24 DK DK01930705T patent/DK1292304T3/da active
- 2001-04-24 HR HR20020909A patent/HRP20020909A2/hr not_active Application Discontinuation
- 2001-04-24 HU HU0300701A patent/HUP0300701A2/hu unknown
- 2001-04-24 ES ES04010651T patent/ES2239558T3/es not_active Expired - Lifetime
- 2001-04-24 DE DE04010651T patent/DE04010651T1/de active Pending
- 2001-04-24 AT AT01930705T patent/ATE308324T1/de not_active IP Right Cessation
- 2001-04-24 DE DE20122435U patent/DE20122435U1/de not_active Expired - Lifetime
- 2001-04-24 CA CA002406982A patent/CA2406982A1/en not_active Abandoned
- 2001-04-24 EP EP01930705A patent/EP1292304B1/en not_active Revoked
- 2001-04-24 AU AU5721301A patent/AU5721301A/xx active Pending
- 2001-04-24 WO PCT/US2001/013175 patent/WO2001080857A1/en not_active Ceased
- 2001-04-24 DE DE04010435T patent/DE04010435T1/de active Pending
- 2001-04-24 JP JP2001577956A patent/JP2003531173A/ja not_active Withdrawn
- 2001-04-24 DE DE60122216T patent/DE60122216T2/de not_active Expired - Fee Related
- 2001-04-24 AU AU2001257213A patent/AU2001257213B2/en not_active Ceased
- 2001-04-24 KR KR1020027014220A patent/KR20030069796A/ko not_active Ceased
- 2001-04-24 SE SE01930705T patent/SE5292304T3/xx unknown
-
2004
- 2004-05-24 US US10/853,338 patent/US20040220212A1/en not_active Abandoned
- 2004-05-24 US US10/853,345 patent/US20040220213A1/en not_active Abandoned
- 2004-05-24 US US10/853,031 patent/US20040220210A1/en not_active Abandoned
- 2004-05-24 US US10/852,912 patent/US20040214858A1/en not_active Abandoned
- 2004-05-24 US US10/853,640 patent/US20040214859A1/en not_active Abandoned
- 2004-05-24 US US10/853,033 patent/US20040220211A1/en not_active Abandoned
-
2006
- 2006-02-09 JP JP2006033099A patent/JP2006137778A/ja active Pending
- 2006-06-27 JP JP2006177160A patent/JP2006249105A/ja active Pending
- 2006-10-25 US US11/588,122 patent/US20070037843A1/en not_active Abandoned
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| JP2006137778A5 (enExample) | ||
| TWI660956B (zh) | 調節蛋白質激酶之化合物的合成 | |
| KR102230628B1 (ko) | 보르티옥세틴 제조 방법 | |
| JP2006519818A5 (enExample) | ||
| JP2020535168A5 (enExample) | ||
| CN1227233C (zh) | 纯晶形的5-氯-3-(4-甲磺酰基苯基)-6′-甲基-[2,3′]联吡啶及其合成方法 | |
| JP2007308494A (ja) | 結晶イマチニブ塩基及びその製造方法 | |
| JP2005503386A5 (enExample) | ||
| JP2013049690A5 (enExample) | ||
| JP2014524442A5 (enExample) | ||
| JP2012500819A5 (enExample) | ||
| JP2005520803A5 (enExample) | ||
| JP2010511649A5 (enExample) | ||
| CN103570633B (zh) | 吉非替尼的制备方法 | |
| JP2016023186A (ja) | シロドシンの製造方法および中間体 | |
| CN101921260B (zh) | 一种伊马替尼的制备方法 | |
| TWI551603B (zh) | 培美曲塞二酸之晶型及其製備方法 | |
| JP2010502682A5 (enExample) | ||
| US20170008848A1 (en) | Methods of making netupitant and intermediates thereof | |
| CN106470984B (zh) | 制备吡虫啉多晶型的方法 | |
| JP2005513122A5 (enExample) | ||
| CN104447758B (zh) | 吡唑并[3,4‑d]嘧啶类化合物的合成工艺 | |
| JP2020517674A (ja) | ボルチオキセチンHBr α型を製造するための方法 | |
| JP2007502883A5 (enExample) | ||
| CN104151238A (zh) | 一种直接制备纯8-羟基喹啉铝的方法 |