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Pyridazines. Part 28. 5-Alkylidene-6-phenyl-3(2H)-pyridazinones, a New Family of Platelet Aggregation Inhibitors.

โœ Scribed by Eddy Sotelo; Nuria Fraiz; Matilde Yanez; Reyes Laguna; Ernesto Cano; Jose Brea; Enrique Ravina

Publisher
John Wiley and Sons
Year
2010
Weight
30 KB
Volume
33
Category
Article
ISSN
0931-7597

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โœฆ Synopsis

Abstract

For Abstract see ChemInform Abstract in Full Text.

๐Ÿ“œ SIMILAR VOLUMES

Pyridazines. XV. Synthesis of 6-aryl-5-a
Pyridazines. XV. Synthesis of 6-aryl-5-amino-3(2H)-pyridazinones as potential platelet aggregation inhibitors
โœ Isabel Estevez; Enrique Raviรฑa; Eddy Sotelo ๐Ÿ“‚ Article ๐Ÿ“… 1998 ๐Ÿ› Journal of Heterocyclic Chemistry ๐ŸŒ English โš– 543 KB

## Abstract Several 3(2__H__)โ€pyridazinones with amino groups at the 5โ€position of the pyridazine nucleus have been prepared. The 6โ€arylโ€5โ€haloโ€3(2__H__)โ€pyridazinones obtained from mucochloric and mucobromic acid lead to the corresponding 5โ€alkylaminoโ€3(2__H__)โ€pyridazinones, which were tested as

ChemInform Abstract: Pyridazines. Part 1
ChemInform Abstract: Pyridazines. Part 15. Synthesis of 6-Aryl-5-amino-3(2H)-pyridazinones as Potential Platelet Aggregation Inhibitors.
โœ Isabel Estevez; Enrique Ravina; Eddy Sotelo ๐Ÿ“‚ Article ๐Ÿ“… 2010 ๐Ÿ› John Wiley and Sons โš– 32 KB ๐Ÿ‘ 1 views

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.