180298-85-5Relevant articles and documents
2-Bromo-1-arylethylidenemalononitriles - Convenient reagents for the regioselective synthesis of fused pyridines
Artyomov, Vasilii A.,Ivanov, Vladimir L.,Shestopalov, Anatolii M.,Litvinov, Victor P.
, p. 13351 - 13360 (2007/10/03)
2-Bromo-1-arylethylidenemalononitriles react with conjugated thiolaronitriles to give products of regioselective S alkylation that can be subsequently involved in the Thorpe reaction. Resulting enaminoacrylonitriles form pyridine ring under base catalysis yielding thienodipyridines. According to this common scheme, functionally substituted thieno[3,2-b]pyridines, thiazolo[4,5-b]pyridines, thieno[3,2-b-4,5-h']dipyridines, their hydrogenated analogues, and pyrido[2',3':4,5]thieno[2.3-d]pyrimidine were synthesized.
2-Bromo-1-phenylethylidenemalononitrile in the synthesis of thieno[3,2-b]pyridines and thiazolo[4,5-b]pyridines
Ivanov,Artemov,Shestopalov,Nesterov,Struchkov,Litvinov
, p. 359 - 364 (2007/10/03)
A novel regioselective synthesis of thieno[3,2-b]pyridines and thiazolo[4,5-b]pyridines from 2-bromo-1-phenylethylidenemalononitrile is proposed. In the case of the thiazolo[4,5-b]pyridines, the intermediate 5-(2,2-dicyano-1-phenylvinyl)thiazoles were separated. Formation of the thiazolo[4,5-b]pyridines was confirmed by x-ray analysis. 1996 Plenum Publishing Corporation.