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2—(2—氯乙酰氨基噻唑—4)—Z—2—甲氧亚胺乙酸的合成[J]. 中国药科大学学报, 1985, (2): 4-6.
引用本文: 2—(2—氯乙酰氨基噻唑—4)—Z—2—甲氧亚胺乙酸的合成[J]. 中国药科大学学报, 1985, (2): 4-6.
SYNTHESIS OF 2-(2-CHLOROACETAMIDOTHIAYOL-4-YL)-(Z)-2-METHOXYIMINO ACETIC ACID[J]. Journal of China Pharmaceutical University, 1985, (2): 4-6.
Citation: SYNTHESIS OF 2-(2-CHLOROACETAMIDOTHIAYOL-4-YL)-(Z)-2-METHOXYIMINO ACETIC ACID[J]. Journal of China Pharmaceutical University, 1985, (2): 4-6.

2—(2—氯乙酰氨基噻唑—4)—Z—2—甲氧亚胺乙酸的合成

SYNTHESIS OF 2-(2-CHLOROACETAMIDOTHIAYOL-4-YL)-(Z)-2-METHOXYIMINO ACETIC ACID

  • 摘要: 以乙酰乙酸乙酯为起始原料,以氯乙酰基为氨基保护基经六步反应合成了2-(2-氯乙酰氨基噻唑-4)-(Z)-2甲氧亚胺乙酸。其顺式异构体的总收率达42.56%,该化合物为制备氨噻肟唑头孢菌素和类似头孢菌素的重要中间原料。

     

    Abstract: 2 - (2 -Chloroacetamidothiazol-4 -yl) - (Z) -2 -methoxyimino acetic acid was synthesized by a six-step method with ethyl acetoacetate as starting meterial. The total yield of the synisomer was increased to 42. 56%.

     

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