GB1355718A - 2-amino-5-chloro-thiazole derivatives - Google Patents
2-amino-5-chloro-thiazole derivativesInfo
- Publication number
- GB1355718A GB1355718A GB2760271A GB2760271A GB1355718A GB 1355718 A GB1355718 A GB 1355718A GB 2760271 A GB2760271 A GB 2760271A GB 2760271 A GB2760271 A GB 2760271A GB 1355718 A GB1355718 A GB 1355718A
- Authority
- GB
- United Kingdom
- Prior art keywords
- amino
- chlorothiazole
- general formula
- reacting
- derivatives
- 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.)
- Expired
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
- C07D277/32—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
-
- 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
- C07D277/46—Acylated amino or imino radicals by carboxylic acids, or sulfur or nitrogen analogues thereof
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Thiazole And Isothizaole Compounds (AREA)
Abstract
1355718 2-Amino-5-chlorothiazole derivatives MELLE-BEZONS 11 June 1971 [11 June 1970] 27602/71 Heading C2C Novel 2-amino-5-chlorothiazole derivatives of the general formula wherein X is O or H 2 and each of R and R<SP>1</SP> is an alkyl, aralkyl, heterocyclic or (heterocyclo)alkyl group or R<SP>1</SP> may be a hydrogen atom or NRR<SP>1</SP> is a heterocyclic group, are prepared (a) when X is O, by reacting 2-chloracetamido-5-chlorothiazole with ammonia or an amine of the general formula R-NH-R<SP>1</SP>; (b) when X is O, by reacting 2-amino-5-chlorothiazole with a glycinyl chloride of the general formula RR<SP>1</SP>NCH 2 - COCl; (c) when X is H 2 , by reacting 2-amino-5- chlorothiazole with a 2-chloroethylamine of the general formula ClCH 2 CH 2 NRR<SP>1</SP>; and (d) when X is H 2 , by reacting N-[2-(2-chloroethyl)amino]- 5-chlorothiazole with an excess of ammonia or an amine of the general formula R-NH-R<SP>1</SP>. Pharmaceutical compositions having antiinflammatory, sedative, tranquillizing and analgesic activity comprise, as active ingredient, a 2-amino-5-chlorothiazole derivative of the first general formula above, in admixture with a pharmacologically acceptable carrier.
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
FR7021383A FR2092714B1 (en) | 1970-06-11 | 1970-06-11 |
Publications (1)
Publication Number | Publication Date |
---|---|
GB1355718A true GB1355718A (en) | 1974-06-05 |
Family
ID=9056998
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
GB2760271A Expired GB1355718A (en) | 1970-06-11 | 1971-06-11 | 2-amino-5-chloro-thiazole derivatives |
Country Status (5)
Country | Link |
---|---|
JP (1) | JPS504664B1 (en) |
DE (1) | DE2128941A1 (en) |
ES (2) | ES392093A1 (en) |
FR (1) | FR2092714B1 (en) |
GB (1) | GB1355718A (en) |
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
EP0005070A2 (en) * | 1978-04-24 | 1979-10-31 | Pfizer Inc. | N-(2-thiazolyl)amides and their use as anti-inflammatory and immunoregulatory agents |
Families Citing this family (7)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS548367U (en) * | 1977-06-20 | 1979-01-19 | ||
JPS5447361U (en) * | 1977-09-08 | 1979-04-02 | ||
FR2572074B1 (en) * | 1984-10-18 | 1987-07-17 | Sanofi Sa | THIADIAZOLE DERIVATIVES ACTIVE IN THE CENTRAL NERVOUS SYSTEM, PROCESS FOR OBTAINING SAME AND PHARMACEUTICAL COMPOSITIONS CONTAINING THEM |
FR2612187B1 (en) * | 1987-03-12 | 1989-07-21 | Sanofi Sa | THIAZOLE DERIVATIVES ACTIVE IN THE CHOLINERGIC SYSTEM, THEIR PREPARATION METHOD AND PHARMACEUTICAL COMPOSITIONS CONTAINING THE SAME |
FR2618780B1 (en) * | 1987-07-29 | 1989-12-08 | Irceba | THIAZOLE DERIVATIVES BELONGING TO THE FAMILY OF 2-PIPERAZINOACETAMIDO-4-METHYLTHIAZOLES, METHOD OF PREPARATION AND THERAPEUTIC USE |
GB9823871D0 (en) * | 1998-10-30 | 1998-12-23 | Pharmacia & Upjohn Spa | 2-Amino-thiazole derivatives, process for their preparation, and their use as antitumour agents |
CA2503844A1 (en) * | 2002-10-30 | 2004-05-21 | Merck & Co., Inc. | Piperidinyl-alpha-aminoamide modulators of chemokine receptor activity |
Family Cites Families (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
FR7428A (en) * |
-
1970
- 1970-06-11 FR FR7021383A patent/FR2092714B1/fr not_active Expired
-
1971
- 1971-06-09 ES ES392093A patent/ES392093A1/en not_active Expired
- 1971-06-09 ES ES392094A patent/ES392094A1/en not_active Expired
- 1971-06-10 JP JP4068671A patent/JPS504664B1/ja active Pending
- 1971-06-11 DE DE19712128941 patent/DE2128941A1/en active Pending
- 1971-06-11 GB GB2760271A patent/GB1355718A/en not_active Expired
Cited By (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
EP0005070A2 (en) * | 1978-04-24 | 1979-10-31 | Pfizer Inc. | N-(2-thiazolyl)amides and their use as anti-inflammatory and immunoregulatory agents |
EP0005070A3 (en) * | 1978-04-24 | 1979-11-28 | Pfizer Inc. | N-(2-thiazolyl)amides and their use as anti-inflammatory and immunoregulatory agents |
Also Published As
Publication number | Publication date |
---|---|
FR2092714A1 (en) | 1972-01-28 |
ES392094A1 (en) | 1974-08-01 |
ES392093A1 (en) | 1974-10-01 |
JPS504664B1 (en) | 1975-02-22 |
FR2092714B1 (en) | 1974-03-22 |
DE2128941A1 (en) | 1971-12-16 |
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Legal Events
Date | Code | Title | Description |
---|---|---|---|
PS | Patent sealed | ||
PLNP | Patent lapsed through nonpayment of renewal fees |