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Synthesis of New 1,3-Thiazolecarbaldehydes

机译:新1,3-噻唑妥甲醛的合成

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摘要

H-Lithiation and Br-lithiation reactions of 1,3-thiazole were studied in order to obtain new thiazole derivatives. Four isomeric chloromethyl derivatives of 1,3-thiazole containing a protected aldehyde group like 2-(1,3-dioxolan-2-yl)-5-(chloromethyl)-1,3-thiazole, 5-(1,3-dioxolan-2-yl)-2-(chloromethyl)-1,3-thiazole, 4-(1,3-dioxolan-2-yl)-2-(chloromethyl)-1,3-thiazole, and 2-(1,3-dioxolan-2-yl)-4-(chloromethyl)-1,3-thiazole were synthesized. Their nucleophilic substitution reactions with dimethylamine and sodium methylthiolate were studied. New aldehydes of 1,3-thiazole series of low-molecular weight were obtained.
机译:研究了1,3-噻唑的H-锂锂化和Br锂锂锂化反应,以获得新的噻唑衍生物。 含有1,3-噻唑的四等异构氯甲基衍生物,其含有受保护的醛基,如2-(1,3-二氧化醇-2-基)-5-(氯甲基)-1,3-噻唑,5-(1,3-二氧杂环 -2-y1)-2-(氯甲基)-1,3-噻唑,4-(1,3-二氧丙烷-2-基)-2-(氯甲基)-1,3-噻唑,和2-(1, 合成3-二氧氧丙-2-基)-4-(氯甲基)-1,3-噻唑。 研究了与二甲胺和甲基硫醇钠的亲核代替反应。 获得了1,3-噻唑系列的新醛的低分子量。

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