【药物名称】
化学结构式(Chemical Structure):
参考文献No.560915
标题:Synthesis and antiinflammatory activity of N-substituted 2-oxo-2H-1-benzopyran-3-carboxamides and their 2-iminoanalagues
作者:Bylov, I.E.; Vasylyev, M.V.; Bilokin, Y.V.
来源:Eur J Med Chem 1999,34(11),997
合成路线图解说明:

By cyclization of 2-hydroxybenzaldehyde (I) with 4-(cyanacetamido)benzoic acid ethyl ester (II) catalyzed by piperidine in ethanol.

合成路线图解说明:

The cyclization of 2-hydroxybenzaldehyde (I) with 2-(cyanacetamido)benzoic acid methyl ester (II) catalyzed by piperidine in ethanol gives the 2-imino-1-benzopyran (III), which is then hydrolyzed to the target benzopyranone with HCl in refluxing ethanol/water.

合成路线图解说明:

The cyclization of 2-hydroxybenzaldehyde (I) with 4-(cyanacetamido)benzoic acid ethyl ester (II) catalyzed by piperidine in ethanol gives the 2-imino-1-benzopyran (III), which is then hydrolyzed to the target benzopyranone with HCl in refluxing ethanol/water.

合成路线图解说明:

By cyclization of 5-chloro-2-hydroxybenzaldehyde (I) with N-(2-carboxyphenyl) malonamic acid ethyl ester (II) catalyzed by piperidine in ethanol.

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