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Improved method of epalrestat synthesis / 浙江大学学报·医学版
Journal of Zhejiang University. Medical sciences ; (6): 356-358, 2003.
Artigo em Chinês | WPRIM | ID: wpr-231048
ABSTRACT
<p><b>OBJECTIVE</b>To synthesize epalrestat and to improve the method of synthesis.</p><p><b>METHODS</b>Glycine reacted with carbondisulfide,then with ClCH(2)COONa to give 3-carboxymethylrhodanine. PhCHO reacted with CH(3)CH(2)CHO in NaOH/EtOH solution to produce 2-methylcinnamaldehyde.3-carboxymethylrhodanine and 2-methylcinnamaldehyde were treated with NH(3).H(2)O to obtain epalrestat.</p><p><b>RESULT</b>The described method was effective in synthesis of Epalrestat and the yield was higher than that of in references.</p><p><b>CONCLUSION</b>The results suggest that this method is suitable for industrial production.</p>
Assuntos
Texto completo: DisponíveL Índice: WPRIM (Pacífico Ocidental) Assunto principal: Rodanina / Aldeído Redutase / Inibidores Enzimáticos / Tiazolidinas Idioma: Chinês Revista: Journal of Zhejiang University. Medical sciences Ano de publicação: 2003 Tipo de documento: Artigo

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Texto completo: DisponíveL Índice: WPRIM (Pacífico Ocidental) Assunto principal: Rodanina / Aldeído Redutase / Inibidores Enzimáticos / Tiazolidinas Idioma: Chinês Revista: Journal of Zhejiang University. Medical sciences Ano de publicação: 2003 Tipo de documento: Artigo