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Efficient synthesis via molecular sieve of 3-(pyrimidin-2yl)- thiazolidinones
Efficient synthesis via molecular sieve of 3-(pyrimidin-2yl)- thiazolidinones
Ribeiro; C.S.; Jr, Campos; J.C.; Bierhals; M.P.; Freitag; R.A.; Cunico; W.; Siqueira; G.M.
Abstract:
Several methods for the synthesis of thiazolidin-4- ones are described in the literature. The most often used involves three components: a primary amine, a carbonyl compound and mercaptoacetic acid using azeotropic distillation with Dean-Stark trap, for the water removal, is the most common approach. Besides, other protocols were developed by using dehydrating agents among these Na2SO4, molecular sieves, DCC and others, with the purpose to improve the yield of the products. The aim of this study was explore the application of molecular sieves in compare with Dean-Satrk trap, as dehydrating agents in the synthesis of 3- (pyrimidin-2-yl)-thiazolidinones.
Several methods for the synthesis of thiazolidin-4- ones are described in the literature. The most often used involves three components: a primary amine, a carbonyl compound and mercaptoacetic acid using azeotropic distillation with Dean-Stark trap, for the water removal, is the most common approach. Besides, other protocols were developed by using dehydrating agents among these Na2SO4, molecular sieves, DCC and others, with the purpose to improve the yield of the products. The aim of this study was explore the application of molecular sieves in compare with Dean-Satrk trap, as dehydrating agents in the synthesis of 3- (pyrimidin-2-yl)-thiazolidinones.
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DOI: 10.5151/chempro-15bmos-BMOS2013_20139160210
Referências bibliográficas
- [1] 1. Jain, A. K.; Vaidya, A.; Ravichandran, V.; Kashaw, S. K.; Agrawal, R. K., Bioorganic And Medicinal Chemistry 2012, 20
- [2] 3378-3395.
- [3] 2. Prasad, D.; Nath, M., J. Heterocycl. Chem. 2012, 49 (3), 628-633.
- [4] 3. Gouvea, D. P.; Bareno, V. D. O.; Bosenbecker, J.; Drawanz, B. B.; Neuenfeldt, P. D.; Siqueira, G. M.; Cunico, W., Ultrason. Sonochem. 2012, 19 (6), 1127-1131. Campos, J. C.; Gouvêa, D. P.; Ribeiro, C. d. S. et al, J Biochem. Mol. Tox. 2013, 27 (9), 445-450.
Como citar:
Ribeiro, ; C.S., ; Jr, Campos; J.C., ; Bierhals, ; M.P., ; Freitag, ; R.A., ; Cunico, ; W., ; Siqueira, ; G.M., ; "Efficient synthesis via molecular sieve of 3-(pyrimidin-2yl)- thiazolidinones", p-14-14.
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_20139160210
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TY - CONF T1 - Efficient synthesis via molecular sieve of 3-(pyrimidin-2yl)- thiazolidinones JO - Blucher Chemistry Proceedings VL - 1 IS - 2 SP - 14 EP - 14 PY - 2013 T2 - Brazilian Meeting on Organic Synthesis 2013 AU - , , , , , , , , , , , SN - 23184043 DO - http://dx.doi.org/10.5151/chempro-15bmos-BMOS2013_20139160210 UR - www.proceedings.blucher.com.br/article-details/efficient-synthesis-via-molecular-sieve-of-3-pyrimidin-2yl-thiazolidinones-8234 KW - ER -
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@article{Ribeiro20144,
title="Efficient synthesis via molecular sieve of 3-(pyrimidin-2yl)- thiazolidinones",
journal="Blucher Chemistry Proceedings",
volume="1",
number="2",
pages="14 - 14",
year="2013",
note="",
issn="23184043",
doi="http://dx.doi.org/10.5151/chempro-15bmos-BMOS2013_20139160210",
url="www.proceedings.blucher.com.br/article-details/efficient-synthesis-via-molecular-sieve-of-3-pyrimidin-2yl-thiazolidinones-8234",
author="5243", "5244", "Campos Jr", "5246", "5247", "5248", "5249", "5250", "5251", "5252", "5253", "5254",
keywords="",
}
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5243, 5244, Campos Jr, 5246, 5247, 5248, 5249, 5250, 5251, 5252, 5253, 5254, Efficient synthesis via molecular sieve of 3-(pyrimidin-2yl)- thiazolidinones, Blucher Chemistry Proceedings, Volume 1, 2013, Pages 14-14, ISSN 23184043, http://dx.doi.org/10.5151/chempro-15bmos-BMOS2013_20139160210 (www.proceedings.blucher.com.br/article-details/efficient-synthesis-via-molecular-sieve-of-3-pyrimidin-2yl-thiazolidinones-8234) Palavras-chave:: ;