FR2302994A1 - 1 Aryl 2 hydroxymethyl cyclopropane carboxylic acids - and lactones, pharmaceutical intermediates - Google Patents
1 Aryl 2 hydroxymethyl cyclopropane carboxylic acids - and lactones, pharmaceutical intermediatesInfo
- Publication number
- FR2302994A1 FR2302994A1 FR7507120A FR7507120A FR2302994A1 FR 2302994 A1 FR2302994 A1 FR 2302994A1 FR 7507120 A FR7507120 A FR 7507120A FR 7507120 A FR7507120 A FR 7507120A FR 2302994 A1 FR2302994 A1 FR 2302994A1
- Authority
- FR
- France
- Prior art keywords
- lactones
- aryl
- pharmaceutical intermediates
- carboxylic acids
- cyclopropane carboxylic
- 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.)
- Granted
Links
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D307/00—Heterocyclic compounds containing five-membered rings having one oxygen atom as the only ring hetero atom
- C07D307/77—Heterocyclic compounds containing five-membered rings having one oxygen atom as the only ring hetero atom ortho- or peri-condensed with carbocyclic rings or ring systems
- C07D307/93—Heterocyclic compounds containing five-membered rings having one oxygen atom as the only ring hetero atom ortho- or peri-condensed with carbocyclic rings or ring systems condensed with a ring other than six-membered
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Abstract
Novel cyclopropane derivs are of formula (I) Ar is phenyl, naphthyl, biphenylyl, pyridyl, furfuryl, thienyl or pyrrolyl gp- opt. monosubstd. by alkyl alkoxy, halogen, NO2, NH2, OH or PhO. The cpds. and their lactones are useful as pharmaceutical intermediates. A typical cpd. is 1-phenyl-2-hydroxymethyl-cyclopropanecarboxylic acid. In an example, this is prepd. by treating benzyl cyanide with NaNH2, reacting the resulting carbanion with epichlorohydrin and hydrolysing the product with KOH.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
FR7507120A FR2302994A1 (en) | 1975-03-06 | 1975-03-06 | 1 Aryl 2 hydroxymethyl cyclopropane carboxylic acids - and lactones, pharmaceutical intermediates |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
FR7507120A FR2302994A1 (en) | 1975-03-06 | 1975-03-06 | 1 Aryl 2 hydroxymethyl cyclopropane carboxylic acids - and lactones, pharmaceutical intermediates |
Publications (2)
Publication Number | Publication Date |
---|---|
FR2302994A1 true FR2302994A1 (en) | 1976-10-01 |
FR2302994B1 FR2302994B1 (en) | 1978-02-03 |
Family
ID=9152239
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
FR7507120A Granted FR2302994A1 (en) | 1975-03-06 | 1975-03-06 | 1 Aryl 2 hydroxymethyl cyclopropane carboxylic acids - and lactones, pharmaceutical intermediates |
Country Status (1)
Country | Link |
---|---|
FR (1) | FR2302994A1 (en) |
Cited By (8)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
FR2421875A1 (en) * | 1978-01-31 | 1979-11-02 | Roussel Uclaf | OPTICALLY ACTIVE SUBSTITUTE BENZYL ALCOHOL AND ITS PREPARATION PROCESS |
US4507318A (en) * | 1981-06-23 | 1985-03-26 | Pierre Fabre S.A. | 1-Aryl 2-aminomethyl cyclopropane carboxylates (Z) as drugs in the treatment of pain |
FR2740452A1 (en) * | 1995-10-25 | 1997-04-30 | Pf Medicament | PROCESS FOR THE MANUFACTURE OF 1-PHENYL-2-OXO-3-OXA-BICYCLO (3: 1: 0) HEXANE |
FR2743559A1 (en) * | 1996-01-16 | 1997-07-18 | Pf Medicament | NOVEL PROCESS FOR THE PREPARATION OF BICYCLIC LACTONS |
WO2005123709A1 (en) * | 2004-06-16 | 2005-12-29 | Sumitomo Chemical Company, Limited | Method for producing 2-oxo-1-phenyl-3-oxabicyclo[3.1.0]hexane |
WO2012145234A3 (en) * | 2011-04-21 | 2012-12-13 | Emory University | Cyclopropyl derivatives and methods of use |
JP2015509939A (en) * | 2012-02-17 | 2015-04-02 | エーザイ・アール・アンド・ディー・マネジメント株式会社 | Methods and compounds useful in the synthesis of orexin-2 receptor antagonists |
CN108205043A (en) * | 2016-12-19 | 2018-06-26 | 成都弘达药业有限公司 | A kind of left-handed detection method of the Milnacipran intermediate in relation to substance |
-
1975
- 1975-03-06 FR FR7507120A patent/FR2302994A1/en active Granted
Cited By (14)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
FR2421875A1 (en) * | 1978-01-31 | 1979-11-02 | Roussel Uclaf | OPTICALLY ACTIVE SUBSTITUTE BENZYL ALCOHOL AND ITS PREPARATION PROCESS |
US4507318A (en) * | 1981-06-23 | 1985-03-26 | Pierre Fabre S.A. | 1-Aryl 2-aminomethyl cyclopropane carboxylates (Z) as drugs in the treatment of pain |
FR2740452A1 (en) * | 1995-10-25 | 1997-04-30 | Pf Medicament | PROCESS FOR THE MANUFACTURE OF 1-PHENYL-2-OXO-3-OXA-BICYCLO (3: 1: 0) HEXANE |
WO1997015563A1 (en) * | 1995-10-25 | 1997-05-01 | Pierre Fabre Medicament | Method for making 1-phenyl-2-oxo-3-oxa-bicyclo (3:1:0) hexane |
FR2743559A1 (en) * | 1996-01-16 | 1997-07-18 | Pf Medicament | NOVEL PROCESS FOR THE PREPARATION OF BICYCLIC LACTONS |
WO1997026256A1 (en) * | 1996-01-16 | 1997-07-24 | Pierre Fabre Medicament | New process for the preparation of bicyclic lactones |
WO2005123709A1 (en) * | 2004-06-16 | 2005-12-29 | Sumitomo Chemical Company, Limited | Method for producing 2-oxo-1-phenyl-3-oxabicyclo[3.1.0]hexane |
AU2005254872B2 (en) * | 2004-06-16 | 2011-04-07 | Sumitomo Chemical Company, Limited | Method for producing 2-oxo-1-phenyl-3-oxabicyclo(3.1.0)hexane |
KR101185278B1 (en) | 2004-06-16 | 2012-09-21 | 스미또모 가가꾸 가부시키가이샤 | Method for producing 2-oxo-1-phenyl-3-oxabicyclo[3.1.0]hexane |
WO2012145234A3 (en) * | 2011-04-21 | 2012-12-13 | Emory University | Cyclopropyl derivatives and methods of use |
US10207984B2 (en) | 2011-04-21 | 2019-02-19 | Emory University | Cyclopropyl derivatives and methods of use |
JP2015509939A (en) * | 2012-02-17 | 2015-04-02 | エーザイ・アール・アンド・ディー・マネジメント株式会社 | Methods and compounds useful in the synthesis of orexin-2 receptor antagonists |
US9828336B2 (en) | 2012-02-17 | 2017-11-28 | Eisai R&D Management Co., Ltd. | Methods and compounds useful in the synthesis of orexin-2 receptor antagonists |
CN108205043A (en) * | 2016-12-19 | 2018-06-26 | 成都弘达药业有限公司 | A kind of left-handed detection method of the Milnacipran intermediate in relation to substance |
Also Published As
Publication number | Publication date |
---|---|
FR2302994B1 (en) | 1978-02-03 |
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Legal Events
Date | Code | Title | Description |
---|---|---|---|
ST | Notification of lapse |