A novel synthesis of 2??arylaminothiazolo [4, 5??d] pyridazinones
T Yamasaki, E Kawaminami, F Uchimura…
Index: Yamasaki, Tetsuo; Kawaminami, Eiji; Uchimura, Fumi; Okawara, Tadashi; Furukawa, Mitsuru Journal of Heterocyclic Chemistry, 1991 , vol. 28, # 4 p. 859 - 865
Full Text: HTML
Citation Number: 3
Abstract
Abstract The reaction of 5 (4)-amino-4 (5)-chloropyridazin-3 (2H)-ones 1 (9) with methyl dithiocarbamates 2 gave 2-arylaminothiazolo [4, 5-d] pyridazinones 3 (10). Treatment of 5 (4)-alkylamino-4 (5)-chloropyridazin-3 (2H)-ones 5 (12) with 2 afforded the corresponding 2- aryliminothiazolo [4, 5-d] pyridazinones 6 (13). Cyclization of 1a with phenylisothiocyanate produced 2-amino-and 2-iminothiazolo [4, 5-d] pyridazinones 3a and 16.
Related Articles:
[Chandrasekhar; Raji Reddy; Jagadeeshwar Rao Tetrahedron, 2001 , vol. 57, # 16 p. 3435 - 3438]
[Yadav, Ganapati D.; Lande, Sharad V. Advanced Synthesis and Catalysis, 2005 , vol. 347, # 9 p. 1235 - 1241]
[Selvam; Balachandran; Velmurugan; Swaminathan Applied Catalysis A: General, 2012 , vol. 413-414, p. 213 - 222]
[Xie, Hui; Ng, Danny; Savinov, Sergey N.; Dey, Barna; Kwong, Peter D.; Wyatt, Richard; Smith III, Amos B.; Hendrickson, Wayne A. Journal of Medicinal Chemistry, 2007 , vol. 50, # 20 p. 4898 - 4908]
[Journal of Medicinal Chemistry, , vol. 27, # 3 p. 347 - 357]