GB847779A - 2-(4-biphenylyl)-í¸-hexenoic acid esters thereof - Google Patents
2-(4-biphenylyl)-í¸-hexenoic acid esters thereofInfo
- Publication number
- GB847779A GB847779A GB12675/59A GB1267559A GB847779A GB 847779 A GB847779 A GB 847779A GB 12675/59 A GB12675/59 A GB 12675/59A GB 1267559 A GB1267559 A GB 1267559A GB 847779 A GB847779 A GB 847779A
- Authority
- GB
- United Kingdom
- Prior art keywords
- biphenylyl
- prepared
- acetonitrile
- hydrocarbon radical
- acid
- 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
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C57/00—Unsaturated compounds having carboxyl groups bound to acyclic carbon atoms
- C07C57/30—Unsaturated compounds having carboxyl groups bound to acyclic carbon atoms containing six-membered aromatic rings
- C07C57/42—Unsaturated compounds having carboxyl groups bound to acyclic carbon atoms containing six-membered aromatic rings having unsaturation outside the rings
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Medicinal Preparation (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Acyclic And Carbocyclic Compounds In Medicinal Compositions (AREA)
Abstract
The invention comprises compounds of the general formula: <FORM:0847779/IV(b)/1> in which R represents a hydrogen atom or a hydrocarbon radical containing up to 10 carbon atoms; and the preparation thereof, where R is hydrogen, by condensing 4-biphenylyl acetic acid nitrile or alkyl ester with crotyl bromide and hydrolysing the product in an alkaline medium or, where R is a hydrocarbon radical, by reacting the corresponding acid chloride, prepared by treating the acid with thionylchloride, with R-OH; and pharmaceutical compositions containing the products. The products are anticholesterinemic agents. 4-Biphenylyl acetonitrile is prepared by reacting 4-biphenylyl methylchloride with an alkali metal cyanide. 2-(4-Biphenylyl)-\se4-hexenoic acid nitrile is prepared by condensing 4-biphenylyl acetonitrile with crotyl bromide. Ethyl 4-biphenylyl-acetate is prepared by treating 4-biphenylyl acetonitrile with ethanol and sulphuric acid.ALSO:Pharmaceutical compositions comprise compounds of the general formula: p <FORM:0847779/VI/1> in which R represents a hydrogen atom or a hydrocarbon radical containing up to 10 carbon atoms, with a pharmaceutical diluent. Oral preparations may be in the form of tablets and capsules.
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US847779XA | 1958-04-14 | 1958-04-14 |
Publications (1)
Publication Number | Publication Date |
---|---|
GB847779A true GB847779A (en) | 1960-09-14 |
Family
ID=22187146
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
GB12675/59A Expired GB847779A (en) | 1958-04-14 | 1959-04-14 | 2-(4-biphenylyl)-í¸-hexenoic acid esters thereof |
Country Status (1)
Country | Link |
---|---|
GB (1) | GB847779A (en) |
Cited By (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US4453005A (en) * | 1982-12-06 | 1984-06-05 | Merck Frosst Canada, Inc. | Process for preparing substituted phenylalkenoic acids |
DE3420387A1 (en) * | 1983-06-03 | 1984-12-06 | Scharper S.p.A. per l'Industria Farmaceutica, Mailand/Milano | 2- (4-BIPHENYLYL) -4-HEXENONIC ACID AND ITS DERIVATIVES WITH ANTI-INFLAMMATORY EFFECTIVENESS |
US4536515A (en) * | 1982-12-06 | 1985-08-20 | Merck Frosst Canada, Inc. | Substituted phenylalkenoic acids and esters |
-
1959
- 1959-04-14 GB GB12675/59A patent/GB847779A/en not_active Expired
Cited By (5)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US4453005A (en) * | 1982-12-06 | 1984-06-05 | Merck Frosst Canada, Inc. | Process for preparing substituted phenylalkenoic acids |
US4536515A (en) * | 1982-12-06 | 1985-08-20 | Merck Frosst Canada, Inc. | Substituted phenylalkenoic acids and esters |
DE3420387A1 (en) * | 1983-06-03 | 1984-12-06 | Scharper S.p.A. per l'Industria Farmaceutica, Mailand/Milano | 2- (4-BIPHENYLYL) -4-HEXENONIC ACID AND ITS DERIVATIVES WITH ANTI-INFLAMMATORY EFFECTIVENESS |
FR2547726A1 (en) * | 1983-06-03 | 1984-12-28 | Scharper Spa | 2- (4-BIPHENYL) -4-HEXENOIC ACID AND DERIVATIVES HAVING ANTI-INFLAMMATORY ACTIVITY |
GB2142015A (en) * | 1983-06-03 | 1985-01-09 | Scharper Spa | 2-(4-biphenylyl)-4-hexenoic acids |
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