Ultrasonics promoted synthesis of thiazolidinones from 2- aminopyridine

Ultrasonics promoted synthesis of thiazolidinones from 2- aminopyridine

Bosenbecker, Juliano; Gouvêa, Daniela P.; Siqueira, Geonir M.; Cunico, Wilson

Abstract:

Thiazolidinones are important five-membered heterocycles that have valuable biological activities in the medicine chemistry. Our research group has been studied non-conventional methodologies for the synthesis of thiazolidinones. Ultrasound irradiation has been utilized to accelerate a number of synthetically useful reactions during the last few years. In continuation of our studies, the aim of this paper is the sonocatalysis synthesis of thiazolidinones from the cyclocondensation reaction of 2-aminopyridine, arenealdehydes and mercaptoacetic acid.

Thiazolidinones are important five-membered heterocycles that have valuable biological activities in the medicine chemistry. Our research group has been studied non-conventional methodologies for the synthesis of thiazolidinones. Ultrasound irradiation has been utilized to accelerate a number of synthetically useful reactions during the last few years. In continuation of our studies, the aim of this paper is the sonocatalysis synthesis of thiazolidinones from the cyclocondensation reaction of 2-aminopyridine, arenealdehydes and mercaptoacetic acid.

Palavras-chave:

DOI: 10.5151/chempro-15bmos-BMOS2013_2013913154444

Referências bibliográficas

• [1] 1 Jain, A.K.; Vaidya, A.; Ravichandran, V.; Kashaw, R.K.A.; Bioorg. Med.
• [2] Chem. 2012, 20, 3378.
• [3] 2 Gouvêa, D.P.; Bareño, V.D.O.; Bosenbecker, J.; Drawanz, B.B.;
• [4] Neuenfeldt, P.D.; Siqueira, G.M.; Cunico, W.; Ultrason. Sonochem. 2012,
• [5] 19, 1127.
• [6] 3 Cravotto, G.; Cintas, P.; Chem. Soc. Ver. 2006, 35, 180.

Como citar:

Bosenbecker, Juliano; Gouvêa, Daniela P.; Siqueira, Geonir M.; Cunico, Wilson; "Ultrasonics promoted synthesis of thiazolidinones from 2- aminopyridine", p-234-234. In: In Blucher Chemistry Proceedings, São Paulo, v. 1, n. 2, Dezembro.2013. São Paulo: Blucher, 2013.
ISSN 23184043, DOI 10.5151/chempro-15bmos-BMOS2013_2013913154444