- Preparation of Triazolopyrimidines as Potential Antiasthma Agents
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With the use of the human basophil histamine release assay, 5-aryl-2-aminotriazolopyrimidines 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 triazolopyrimidines, after a Dimroth rearrangement.Following a structure-activity evaluation, the5--2-amino (8-10), 5-(3-bromophenyl)-2-amino (8-13), 5--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.
- Medwid, Jeffrey B.,Paul, Rolf,Baker, Jannie S.,Brockman, John A.,Du, Mila T.,et al.
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p. 1230 - 1241
(2007/10/02)
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- Reduction of 3-Amino-1,2-benzisothiazoles and 3-Imino-1,2-benzisothiazolines to 2-Mercaptobenzamidines, Benzamidiniumthiolates, or 1,2-Benzothioquinone Methides
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The 2-mercaptobenzamidines 4 are formed by reduction of the 3-amino-1,2-benzisothiazoles 1 or 3-imino-1,2-benzisothiazolines 2.They can be described as 2-mercaptobenzamidines 4, benzamidiniumthiolates 4', and 1,2-benzothioquinone methides 4'' (a canonical
- Boeshagen, Horst,Geiger, Walter
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