122001-78-9Relevant articles and documents
Pyridazine derivatives, VII. Synthesis and hypotensive activity of 3-hydrazinocycloalkyl[1,2-c]pyridazines and their derivatives.
Teran,Ravina,Santana,Garcia-Dominguez,Garcia-Mera,Fontenla,Orallo,Calleja
, p. 331 - 336 (1989)
The preparation of a series of 3-hydrazinocycloalkyl[1,2-c]pyridazines 7 and some derivatives as hydrazones 8, 9, triazoles 10 and pyrroles 11 are described together with their hypotensive activity in normotensive rats.
Preparation of cycloalkano[c]pyridazinones and cycloalkane-condensed pyrrolo[1,2-a]imidazolone, -pyrimidinone and -[1,3]diazepinone stereoisomers
Csende, Ferenc,Bernath, Gabor,Boecskei, Zsolt,Sohar, Pal,Stajer, Geza
, p. 323 - 330 (2007/10/03)
From the 2-ethoxycarbonylmethyl-1-cycloalkanones (1a-c) with hydrazine, the cyclopenta- (2a), cyclohexa- (2b) and cyclohepta[c]pyridazinones (2c) were prepared. 2a-c were transformed to the corresponding dehydro derivatives (3a-c) by means of a recently-developed smooth oxidation method with CuCl2 in acetonitrile. Compounds (1) reacted with α,ω-alkylenediamines to furnish saturated cycloalkano[6]pyrrolo[1,2-cr]diazinones (4a-f). The structures of 4a-f were determined by 1H- and 13C-NMR methods, including DNOE, DEPT and 2D-HSC measurements, and for 4a also by X-ray analysis. The rings of the 2-perhydroindolone and its homologues are cis-fused, while the NH group of the heterocycle containing two N atoms and the annelational hydrogen are cis in all compounds prepared.
