7,10-Dichloro-3-methyl-4-phenyl-1,2,3,4-tetrahydrobenz[H]isoquinoline hydrobromide

Information

  • Patent Grant
  • 4205172
  • Patent Number
    4,205,172
  • Date Filed
    Monday, January 8, 1979
    45 years ago
  • Date Issued
    Tuesday, May 27, 1980
    44 years ago
Abstract
The compound 7,10-dichloro-3-methyl-4-phenyl-1,2,3,4-tetrahydrobenz[h]isoquinoline hydrobromide is useful as an antifungal agent.
Description

The invention is concerned with the compound 7,10-dichloro-3-methyl-4-phenyl-1,2,3,4-tetrahydrobenz[h]isoquinoline hydrobromide. At a concentration of 40 .mu.g/ml and 100 .mu.g/ml in Sabourand's dextrose broth it inhibits the growth of Candida albicans and Microsporum canis, respectively, in the commonly employed agar diffusion test. It is adapted to be combined in various forms such as elixirs, dust, unguents, solutions and suspensions to provide compositions inimical to fungal growth.





In order that this invention may be readily available to and understood by those skilled in the art, the following preparation is supplied.
7,10-Dichloro-3-methyl-4-phenyl-1,2,3,4-tetrahydrobenz[h]isoquinoline hydrobromide
To 34.0 g (0.0944 mole) of 2-(5,8-dichloro-1-naphthylmethylamino)-1-phenyl-1-propanol free base was added cautiously 250 ml 48% HBr. The mixture was stirred and refluxed for sixty hours, cooled and the resulting solid was filtered through a medium sintered glass funnel. The solid was washed with 3.times.75 ml H.sub.2 O, air dried for three hours, washed with 3.times.125 ml ethyl acetate, and air dried. The product weighed 27.9 g (70%) and melted at 298-310.degree.. An analytical sample, m.p. 313-317.degree., was obtained by recrystallization from methanol.
Anal. calcd. for C.sub.20 H.sub.17 Cl.sub.2 N.HBr: C, 56.76; H, 4.29; N, 3.31. Found: C, 56.87; H, 4.23; N, 3.12.
Claims
  • 1. The compound 7,10-dichloro-3-methyl-4-phenyl-1,2,3,4-tetrahydrobenz[h]isoquinoline hydrobromide.
US Referenced Citations (3)
Number Name Date Kind
3940400 Schwan Feb 1976
4081543 Bastion Mar 1978
4115387 Schwan Sep 1978