GB845500A - Novel acetophenone and iú¾ú´quinoline derivatives and a process for the manufacture thereof - Google Patents

Novel acetophenone and iú¾ú´quinoline derivatives and a process for the manufacture thereof

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Publication number
GB845500A
GB845500A GB4211/59A GB421159A GB845500A GB 845500 A GB845500 A GB 845500A GB 4211/59 A GB4211/59 A GB 4211/59A GB 421159 A GB421159 A GB 421159A GB 845500 A GB845500 A GB 845500A
Authority
GB
United Kingdom
Prior art keywords
acetamido
ethyl
dimethoxy
formula
methylene
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
Application number
GB4211/59A
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
F Hoffmann La Roche AG
Original Assignee
F Hoffmann La Roche AG
Priority date (The priority date 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 date listed.)
Filing date
Publication date
Application filed by F Hoffmann La Roche AG filed Critical F Hoffmann La Roche AG
Publication of GB845500A publication Critical patent/GB845500A/en
Expired legal-status Critical Current

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  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
  • Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)

Abstract

The invention comprises compounds of the formula: <FORM:0845500/IV(b)/1> where R1, R2 and R3 are alkyl or alkoxy groups (any adjacent pair of which alkoxy groups may be combined as alkylenedioxy) and R4 is an alkyl group and where the broken lines denote that the group attached is optional. The compounds may be prepared by acylating an isoquinoline compound of the formula: <FORM:0845500/IV(b)/2> to give the 1-methylene derivative of the formula: <FORM:0845500/IV(b)/3> which is then treated with a dilute mineral acid to open the nitrogen containing ring. The acylation may be carried out by means of an acid anhydride e.g. acetic, propionic or benzoic anhydride and the 1-methylene intermediate need not be isolated. Examples describe the preparation of (1) 2-(b -acetamido-ethyl)-4,5-dimethoxy, (2) 2-(b -propionylamido-ethyl)-4,5-dimethoxy, (3) 2-(b -benzamido-ethyl)-4,5-dimethoxy, (4)2-(b -acetamido-propyl)-4,5-dimethoxy, (5) 2-(b -acetamido-propyl)-4,5-dimethyl, (6) 2-(b -acetamido-ethyl)-4-methoxy, (7) 2-(b -acetamidoethyl)-4,5-methylenedioxy, and (8) 2-(b -acetamido-ethyl)-4,5,6-trimethoxy acetophenone. The preparation of the methylene intermediates is also described.
GB4211/59A 1958-02-14 1959-02-06 Novel acetophenone and iú¾ú´quinoline derivatives and a process for the manufacture thereof Expired GB845500A (en)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
CH845500X 1958-02-14

Publications (1)

Publication Number Publication Date
GB845500A true GB845500A (en) 1960-08-24

Family

ID=4541776

Family Applications (1)

Application Number Title Priority Date Filing Date
GB4211/59A Expired GB845500A (en) 1958-02-14 1959-02-06 Novel acetophenone and iú¾ú´quinoline derivatives and a process for the manufacture thereof

Country Status (1)

Country Link
GB (1) GB845500A (en)

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