Synthesis of 6-Aryl-5-amino-3(2H)pyridazinones as Potential Platelet Aggregation Inhibitors. -Several 3(2H)-pyridazinones (III), (V), (VII), (IX), (XI) with amino groups at the 5-position are prepared starting from mucochloric or mucobromic acids (I) and tested as platelet aggregation inhibitors.
Pyridazines. XV. Synthesis of 6-aryl-5-amino-3(2H)-pyridazinones as potential platelet aggregation inhibitors
✍ Scribed by Isabel Estevez; Enrique Raviña; Eddy Sotelo
- Publisher
- Journal of Heterocyclic Chemistry
- Year
- 1998
- Tongue
- English
- Weight
- 543 KB
- Volume
- 35
- Category
- Article
- ISSN
- 0022-152X
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✦ Synopsis
Abstract
Several 3(2__H__)‐pyridazinones with amino groups at the 5‐position of the pyridazine nucleus have been prepared. The 6‐aryl‐5‐halo‐3(2__H__)‐pyridazinones obtained from mucochloric and mucobromic acid lead to the corresponding 5‐alkylamino‐3(2__H__)‐pyridazinones, which were tested as platelet aggregation inhibitors.
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