Substd phenylacetic acid esters analgesic anti

Cpds. of general formula (I) - R1=H, Me, or Et - R2=H, F, Cl, or Br - R3 and R4=(1-4C) alkyl, or NR3R4 forms a (4-6C) polymethyleneimino residue, or a morpholino group - A=(2-3C) alkylene with at least 2C atoms between O and N. - B) Salts of I - C) Some cpds. III. - Analgesics, antiphlogistics, and...

Full description

Saved in:
Bibliographic Details
Main Authors OSTERMAYER,FRANZ,DR, DENSS,ROLF,DR, CLAUSON-KAAS,NIELS
Format Patent
LanguageEnglish
German
Published 28.02.1971
Edition1
Subjects
Online AccessGet full text

Cover

Loading…
More Information
Summary:Cpds. of general formula (I) - R1=H, Me, or Et - R2=H, F, Cl, or Br - R3 and R4=(1-4C) alkyl, or NR3R4 forms a (4-6C) polymethyleneimino residue, or a morpholino group - A=(2-3C) alkylene with at least 2C atoms between O and N. - B) Salts of I - C) Some cpds. III. - Analgesics, antiphlogistics, and musculotropic-spasmolytics. Dose 50-3000 mg. - Sodium 2-(p-(1-pyrryl)phenyl)butyrate (3.0 g) and 2-piperidinoethyl chloride (2.0 g) were refluxed 15 hr. in PhMe, cooled, washed with H2O (2 x 10 ml), evapd. in vac. and distilled at 0.02 mm, bath temp. 240-250 deg. The distillate in Et2O was treated with 2.8N HCl/Et2O (4 ml), giving I HCl, m.p 114-7 deg. (from butanone).
Bibliography:Application Number: CH19700016411