Journal of Medicinal Chemistry p. 1230 - 1241 (1990)
Update date:2022-07-29
Topics:
Medwid, Jeffrey B.
Paul, Rolf
Baker, Jannie S.
Brockman, John A.
Du, Mila T.
et al.
With the use of the human basophil histamine release assay, 5-aryl-2-amino<1,2,4>triazolo<1,5-c>pyrimidines were found to be active as mediator release inhibitors.These compounds were prepared by reacting arylamidines with sodium ethyl formylacetate or with ethyl propiolate to give pyrimidinones.Treatment with phosphorus oxychloride gave a chloropyrimidine, which was converted to a hydrazinopyrimidine with hydrazine.Cyclization, using cyanogen bromide, gave the triazolo<1,5-c>pyrimidines, after a Dimroth rearrangement.Following a structure-activity evaluation, the5-<3-(trifluoromethyl)phenyl>-2-amino (8-10), 5-(3-bromophenyl)-2-amino (8-13), 5-<3-(difluoromethoxy)phenyl>-2-amino (8-11), and 5-(4-pyridinyl)-2-amino (6-7) compounds were found to have the best activity.They were chosen for further pharmacological and toxicological study.
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