Heterocyclic amplifiers of phleomycin. IV. Pyrimidinylpurines, phenylpyrimidines and related systems with basic side chains
- 1 January 1984
- journal article
- research article
- Published by CSIRO Publishing in Australian Journal of Chemistry
- Vol. 37 (10) , 2093-2101
- https://doi.org/10.1071/ch9842093
Abstract
Syntheses of 4,5,6-triamino-2,4'-bipyrimidines and subsequent conversions into 6-amino-2-pyrimidinylpurine-8-thiones, and their S-dimethylaminoethyl derivatives, are described; routes to a series of cyclohexyl- and piperidino-pyrimidines bearing a sulfur-linked side chain, as well as to phenyl- and methyl-pyrimidines bearing two such side chains, are also described. As amplifiers of phleomycin in a bacterial screen, the above purines proved poor, the cyclohexyl- and piperidinopyrimidines showed medium activities, and the phenylpyrimidines with two side chains (but not the analogous methylpyrimidines) exhibited very high activities.Keywords
This publication has 2 references indexed in Scilit:
- Unfused heterobicycles as amplifiers of phleomycin. VI. Some thienyl- and thiazolyl-pyrimidines with strongly basic side chainsAustralian Journal of Chemistry, 1982
- Unfused heterobicycles as amplifiers of phleomycin. V. A range of pyridinylpyrimidines with strongly basic side chainsAustralian Journal of Chemistry, 1982