摘要
以3-氯磺酰基-2-甲氧羰基噻吩为原料,用甘氨酸甲酯盐酸盐代替肌氨酸甲酯盐酸盐,经缩合、闭环、与硫酸二甲酯进行N-甲基化反应合成了替诺昔康的中间体4-羟基-2-甲基-2H-噻吩并[2,3-e]-1,2-噻嗪-3-甲酸甲酯-1,1-二氧化物。通过1HNMR确认了产物的结构。
The intermediate of tenoxicam, 4-hydroxy-2-methy1-2H-thieno [2,3-e]-1,2-thiazine-3- carboxylate-1,1-dioxide, was synthesized from 3 - (chlorosulfonyl) - 2 - thiophenecarboxylate and glyeine methyl ester hydrochloride instead of sareosine methyl ester hydroehloride by condensation, cyclization and N - methylation with dimethyl sulfate. The structures of the products were confirmed by ^1H NMR.
出处
《山东化工》
CAS
2009年第3期23-26,共4页
Shandong Chemical Industry
关键词
替诺昔康
中间体
缩合
合成
tenoxicam
intermediate
condensation
synthesis