FI873346A - Foerfarande foer framstaellning av morfologiskt homogena former av thiazolderivat. - Google Patents
Foerfarande foer framstaellning av morfologiskt homogena former av thiazolderivat. Download PDFInfo
- Publication number
- FI873346A FI873346A FI873346A FI873346A FI873346A FI 873346 A FI873346 A FI 873346A FI 873346 A FI873346 A FI 873346A FI 873346 A FI873346 A FI 873346A FI 873346 A FI873346 A FI 873346A
- Authority
- FI
- Finland
- Prior art keywords
- thiazolderivat
- morfologiskt
- homogena
- former
- foerfarande foer
- Prior art date
Links
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D277/00—Heterocyclic compounds containing 1,3-thiazole or hydrogenated 1,3-thiazole rings
- C07D277/02—Heterocyclic compounds containing 1,3-thiazole or hydrogenated 1,3-thiazole rings not condensed with other rings
- C07D277/20—Heterocyclic compounds containing 1,3-thiazole or hydrogenated 1,3-thiazole rings not condensed with other rings having two or three double bonds between ring members or between ring members and non-ring members
- C07D277/22—Heterocyclic compounds containing 1,3-thiazole or hydrogenated 1,3-thiazole rings not condensed with other rings having two or three double bonds between ring members or between ring members and non-ring members with only hydrogen atoms, hydrocarbon or substituted hydrocarbon radicals, directly attached to ring carbon atoms
- C07D277/28—Radicals substituted by nitrogen atoms
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D277/00—Heterocyclic compounds containing 1,3-thiazole or hydrogenated 1,3-thiazole rings
- C07D277/02—Heterocyclic compounds containing 1,3-thiazole or hydrogenated 1,3-thiazole rings not condensed with other rings
- C07D277/20—Heterocyclic compounds containing 1,3-thiazole or hydrogenated 1,3-thiazole rings not condensed with other rings having two or three double bonds between ring members or between ring members and non-ring members
- C07D277/32—Heterocyclic compounds containing 1,3-thiazole or hydrogenated 1,3-thiazole rings not condensed with other rings having two or three double bonds between ring members or between ring members and non-ring members 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
- C07D277/38—Nitrogen atoms
- C07D277/44—Acylated amino or imino radicals
- C07D277/48—Acylated amino or imino radicals by radicals derived from carbonic acid, or sulfur or nitrogen analogues thereof, e.g. carbonylguanidines
-
- 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
- A61P1/04—Drugs for disorders of the alimentary tract or the digestive system for ulcers, gastritis or reflux esophagitis, e.g. antacids, inhibitors of acid secretion, mucosal protectants
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P43/00—Drugs for specific purposes, not provided for in groups A61P1/00-A61P41/00
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D277/00—Heterocyclic compounds containing 1,3-thiazole or hydrogenated 1,3-thiazole rings
- C07D277/02—Heterocyclic compounds containing 1,3-thiazole or hydrogenated 1,3-thiazole rings not condensed with other rings
- C07D277/20—Heterocyclic compounds containing 1,3-thiazole or hydrogenated 1,3-thiazole rings not condensed with other rings having two or three double bonds between ring members or between ring members and non-ring members
- C07D277/32—Heterocyclic compounds containing 1,3-thiazole or hydrogenated 1,3-thiazole rings not condensed with other rings having two or three double bonds between ring members or between ring members and non-ring members 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
- C07D277/38—Nitrogen atoms
- C07D277/42—Amino or imino radicals substituted by hydrocarbon or substituted hydrocarbon radicals
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Health & Medical Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Life Sciences & Earth Sciences (AREA)
- General Chemical & Material Sciences (AREA)
- Medicinal Chemistry (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Pharmacology & Pharmacy (AREA)
- Engineering & Computer Science (AREA)
- Animal Behavior & Ethology (AREA)
- General Health & Medical Sciences (AREA)
- Public Health (AREA)
- Veterinary Medicine (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Thiazole And Isothizaole Compounds (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
HU337086 | 1986-08-05 | ||
HU863370A HU196775B (en) | 1986-08-05 | 1986-08-05 | Process for production of morfologically unique new modifications of famotidin and medical compositions containing such substances |
Publications (4)
Publication Number | Publication Date |
---|---|
FI873346A0 FI873346A0 (fi) | 1987-08-03 |
FI873346A true FI873346A (fi) | 1988-02-06 |
FI89917B FI89917B (fi) | 1993-08-31 |
FI89917C FI89917C (fi) | 1993-12-10 |
Family
ID=10963778
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
FI873346A FI89917C (fi) | 1986-08-05 | 1987-08-03 | Foerfarande foer framstaellning av de morfologiskt homogena formerna av famotidin |
Country Status (18)
Country | Link |
---|---|
US (3) | US4894459A (fi) |
EP (1) | EP0256747B2 (fi) |
JP (2) | JP2644234B2 (fi) |
KR (1) | KR940003954B1 (fi) |
CN (1) | CN1024275C (fi) |
AR (1) | AR243175A1 (fi) |
AT (1) | ATE82274T1 (fi) |
AU (1) | AU604040B2 (fi) |
BG (1) | BG60496B2 (fi) |
CA (1) | CA1265809A (fi) |
CS (1) | CS268188B2 (fi) |
DE (2) | DE3782576T3 (fi) |
DK (1) | DK175022B1 (fi) |
FI (1) | FI89917C (fi) |
GR (1) | GR871216B (fi) |
HU (1) | HU196775B (fi) |
PH (1) | PH24069A (fi) |
PT (1) | PT85473B (fi) |
Families Citing this family (26)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
IL86330A0 (en) * | 1987-06-22 | 1988-11-15 | Marga Investigacion | Famotidine polymorphic forms and their preparation |
DE69429119T2 (de) * | 1993-07-09 | 2002-07-18 | R.P. Scherer Corp., Troy | Verfahren zur herstellung von gefriergetrockneten arzneistoffdosierungsformen |
US6756379B2 (en) | 2001-07-26 | 2004-06-29 | Taro Pharmaceutical Industries Ltd. | Non-sedating barbiturate compounds as neuroprotective agents |
US6939873B2 (en) * | 2000-07-26 | 2005-09-06 | Taro Pharmaceuticals Industries Limited | Non-sedating barbituric acid derivatives |
US7683071B2 (en) * | 2000-07-26 | 2010-03-23 | Taro Pharmaceuticals Industries Ltd. | Composition and method for improved bioavailability and enhanced brain delivery of 5,5-diphenyl barbituric acid |
TWI353979B (en) * | 2002-04-10 | 2011-12-11 | Nippon Zoki Pharmaceutical Co | Novel crystal form of 5-hydroxy-1-methylhydantoin |
CA2426122A1 (en) * | 2002-05-02 | 2003-11-02 | M/S Tonira Pharma Limited | A process for the preparation of a combination of famotidine polymorphis a and b |
AR040661A1 (es) * | 2002-07-26 | 2005-04-13 | Theravance Inc | Diclorhidrato cristalino de n-{2-[-((r)-2-hidroxi-2-feniletilamino)fenil]etil}-(r)-2hidroxi-2-(3-formamido-4-hidroxifenil)etilamina, agonista del receptor adrenergico beta 2 |
BR0317289A (pt) | 2002-12-11 | 2005-11-08 | Taro Pharma Ind | Método para tratar distúrbios do movimento usando derivados do ácido barbitúrico |
TW200510277A (en) * | 2003-05-27 | 2005-03-16 | Theravance Inc | Crystalline form of β2-adrenergic receptor agonist |
CA2572797A1 (en) * | 2004-07-02 | 2006-01-12 | Daniella Gutman | A process for preparing 1-methoxymethyl-5,5-diphenylbarbituric acid |
CN101257800B (zh) * | 2005-07-18 | 2012-07-18 | 好利用医疗公司 | 包含法莫替丁和布洛芬的药物 |
US8067451B2 (en) * | 2006-07-18 | 2011-11-29 | Horizon Pharma Usa, Inc. | Methods and medicaments for administration of ibuprofen |
US20080020040A1 (en) * | 2006-07-18 | 2008-01-24 | Horizon Therapeutics, Inc. | Unit dose form for administration of ibuprofen |
US20080021078A1 (en) * | 2006-07-18 | 2008-01-24 | Horizon Therapeutics, Inc. | Methods and medicaments for administration of ibuprofen |
US8067033B2 (en) * | 2007-11-30 | 2011-11-29 | Horizon Pharma Usa, Inc. | Stable compositions of famotidine and ibuprofen |
JP2009543885A (ja) | 2006-07-18 | 2009-12-10 | ホライゾン セラピューティクス, インコーポレイテッド | イブプロフェンの投与のための方法および医薬 |
EP2063873A2 (en) * | 2006-08-31 | 2009-06-03 | Horizon Therapeutics, Inc. | Nsaid dose unit formulations with h2-receptor antagonists and methods of use |
US8039461B1 (en) | 2006-11-10 | 2011-10-18 | Pisgah Laboratories, Inc. | Physical states of a pharmaceutical drug substance |
US7718649B1 (en) | 2006-11-10 | 2010-05-18 | Pisgah Labs, Inc. | Physical states of a pharmaceutical drug substance |
WO2008066704A2 (en) * | 2006-11-14 | 2008-06-05 | Taro Pharmaceuticals North America, Inc. | Method of improving bioavailability for non-sedating barbiturates |
US8883863B1 (en) | 2008-04-03 | 2014-11-11 | Pisgah Laboratories, Inc. | Safety of psuedoephedrine drug products |
TW201011043A (en) | 2008-06-20 | 2010-03-16 | Chugai Pharmaceutical Co Ltd | Crystal of spiroketal derivatives and process for preparation of spiroketal derivatives |
WO2015163832A1 (en) | 2014-04-25 | 2015-10-29 | Pharmacti̇ve İlaç Sanayi̇ Ve Ti̇caret A.Ş. | An ibuprofen and famotidine combined composition having improved stability |
TR201618765A2 (tr) | 2016-12-16 | 2018-07-23 | Imuneks Farma Ilac Sanayi Ve Ticaret Anonim Sirketi | Ağrı ve enflamasyonun tedavisi için steroid olmayan anti-enflamatuvar ilaçlar ve H2 reseptörü antagonisti kombinasyonları. |
CN116194102A (zh) | 2020-07-15 | 2023-05-30 | 沙巴研究联合有限责任公司 | 用于治疗急性疼痛和降低胃灼热的严重程度和/或风险的包含布洛芬和法莫替丁的单位口服剂量组合物 |
Family Cites Families (10)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
GB1543238A (en) * | 1976-09-21 | 1979-03-28 | Smith Kline French Lab | Polymorph of cimetidine |
JPS6056143B2 (ja) * | 1979-08-02 | 1985-12-09 | 山之内製薬株式会社 | アミジン誘導体ならびにその製造法 |
JPS5655383A (en) * | 1979-10-12 | 1981-05-15 | Yamanouchi Pharmaceut Co Ltd | Amizine derivative and its preparation |
HU185457B (en) * | 1981-09-25 | 1985-02-28 | Richter Gedeon Vegyeszet | Process for preparating cimetidine-z |
US4496737A (en) * | 1982-09-27 | 1985-01-29 | Merck & Co., Inc. | Process for preparing sulfamylamidine antisecretory agents |
JPS59227870A (ja) * | 1983-06-07 | 1984-12-21 | Yamanouchi Pharmaceut Co Ltd | 新規2−グアニジノチアゾリン誘導体ならびにその製造法 |
HU194845B (en) * | 1985-09-11 | 1988-03-28 | Richter Gedeon Vegyeszet | Process for production of n-sulphamil-3-/2-guanidintiazolil-4-methil-tio/-propion-amidin |
DE3644246A1 (de) * | 1986-06-20 | 1987-12-23 | Uriach & Cia Sa J | Verfahren zur herstelung von 3-(((2-((aminoiminomethyl)-amino)-4-thiazolyl)-methyl)-thio)-n-(aminosulfonyl)-propanimidamid |
GB8618847D0 (en) * | 1986-08-01 | 1986-09-10 | Smith Kline French Lab | Pharmaceutical formulations |
IL86330A0 (en) * | 1987-06-22 | 1988-11-15 | Marga Investigacion | Famotidine polymorphic forms and their preparation |
-
1986
- 1986-08-05 HU HU863370A patent/HU196775B/hu unknown
-
1987
- 1987-07-29 GR GR871216A patent/GR871216B/el unknown
- 1987-07-30 PH PH35602A patent/PH24069A/en unknown
- 1987-08-03 DK DK198704041A patent/DK175022B1/da not_active IP Right Cessation
- 1987-08-03 PT PT85473A patent/PT85473B/pt unknown
- 1987-08-03 FI FI873346A patent/FI89917C/fi not_active IP Right Cessation
- 1987-08-04 CS CS875799A patent/CS268188B2/cs not_active IP Right Cessation
- 1987-08-04 JP JP62193855A patent/JP2644234B2/ja not_active Expired - Lifetime
- 1987-08-04 KR KR1019870008563A patent/KR940003954B1/ko not_active IP Right Cessation
- 1987-08-04 CA CA000543728A patent/CA1265809A/en not_active Expired - Lifetime
- 1987-08-04 US US07/081,423 patent/US4894459A/en not_active Expired - Lifetime
- 1987-08-04 DE DE3782576T patent/DE3782576T3/de not_active Expired - Lifetime
- 1987-08-04 EP EP87306882A patent/EP0256747B2/en not_active Expired - Lifetime
- 1987-08-04 AR AR87308333A patent/AR243175A1/es active
- 1987-08-04 DE DE198787306882T patent/DE256747T1/de active Pending
- 1987-08-04 AT AT87306882T patent/ATE82274T1/de not_active IP Right Cessation
- 1987-08-04 AU AU76542/87A patent/AU604040B2/en not_active Expired
- 1987-08-04 CN CN87105373A patent/CN1024275C/zh not_active Expired - Lifetime
-
1990
- 1990-04-27 US US07/515,191 patent/US5120850A/en not_active Expired - Lifetime
-
1991
- 1991-07-11 US US07/728,805 patent/US5128477A/en not_active Expired - Lifetime
-
1994
- 1994-01-18 BG BG098384A patent/BG60496B2/bg unknown
- 1994-08-22 JP JP6196865A patent/JP2708715B2/ja not_active Expired - Lifetime
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Legal Events
Date | Code | Title | Description |
---|---|---|---|
BB | Publication of examined application | ||
FG | Patent granted |
Owner name: RICHTER GEDEON VEGYESZETI GYAR R.T. |
|
MA | Patent expired |