Preparation of 7,8-dimethoxy-3,4-dihydroisoquinoline, facile route to 7,8-dioxygenated-3,4-dihydroisoquinolines.

Abstract:

:Oxidation of 7,8-dimethoxy-1,2,3,4-tetrahydroisoquinoline with potassium permanganate in acetone afforded 7,8-dimethoxy-3,4-dihydroisoquinoline as the primary product. Hence, oxidation of the appropriate secondary nonphenolic 7,8-dioxygenated tetrahydroisoquinoline alkaloid is thus a facile method for the generation of the corresponding imine. The imine is not easily prepared via the usual synthetic route involving ring closure of beta-phenethylamine derivatives.

journal_name

J Pharm Sci

authors

el-Fishawy AM,Slatkin DJ,Knapp JE,Schiff PL Jr

doi

10.1002/jps.2600731137

subject

Has Abstract

pub_date

1984-11-01 00:00:00

pages

1639-40

issue

11

eissn

0022-3549

issn

1520-6017

pii

S0022-3549(15)46422-6

journal_volume

73

pub_type

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