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新型生物活性4-羟基-N'-(亚苄基)-2H-苯并[e][1,2]噻嗪-3-碳酰肼1,1-二氧化物的简便合成方法。

A facile synthesis of novel biologically active 4-hydroxy-N'-(benzylidene)-2H-benzo[e][1,2]thiazine-3-carbohydrazide 1,1-dioxides.

作者信息

Zia-ur-Rehman Muhammad, Choudary Jamil Anwar, Elsegood Mark Robert James, Siddiqui Hamid Latif, Khan Khalid Mohammad

机构信息

Applied Chemistry Research Centre, PCSIR Laboratories Complex, Ferozpur Road, Lahore, Punjab 54600, Pakistan.

出版信息

Eur J Med Chem. 2009 Mar;44(3):1311-6. doi: 10.1016/j.ejmech.2008.08.002. Epub 2008 Aug 13.

Abstract

A novel series of potentially biologically active 4-hydroxy-N'-(benzylidene)-2H-benzo[e][1,2]thiazine-3-carbohydrazide 1,1-dioxides were synthesized starting from ultrasonic mediated N-alkylation of sodium saccharin with methyl chloroacetate. Ring expansion of methyl(1,1-dioxido-3-oxo-1,2-benzisothiazol-2(3H)-yl)acetate followed by its hydrazinolysis afforded 4-hydroxy-2H-1,2-benzothiazine-3-carbohydrazide 1,1-dioxide which was reacted in a straight forward manner with various benzaldehydes in an ultrasonic bath to get the title compounds. All of the synthesized compounds were subjected to preliminary evaluation for their antibacterial and DPPH radical scavenging activities.

摘要

以超声介导的糖精钠与氯乙酸甲酯的N-烷基化反应为起始步骤,合成了一系列新型的具有潜在生物活性的4-羟基-N'-(亚苄基)-2H-苯并[e][1,2]噻嗪-3-碳酰肼1,1-二氧化物。(1,1-二氧代-3-氧代-1,2-苯并异噻唑-2(3H)-基)乙酸甲酯进行扩环反应,随后进行肼解反应,得到4-羟基-2H-1,2-苯并噻嗪-3-碳酰肼1,1-二氧化物,该化合物在超声浴中与各种苯甲醛直接反应,得到目标化合物。对所有合成的化合物进行了抗菌和DPPH自由基清除活性的初步评估。

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