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【结 构 式】

【分子编号】28169

【品名】1-methyl-1H-pyrrole-2-carbonyl chloride

【CA登记号】

【 分 子 式 】C6H6ClNO

【 分 子 量 】143.57248

【元素组成】C 50.19% H 4.21% Cl 24.69% N 9.76% O 11.14%

与该中间体有关的原料药合成路线共 1 条

合成路线1

该中间体在本合成路线中的序号:(VII)

The reaction of acid (I) with SOCl2 in ethyl ether containing triethylamine gives the corresponding acyl chloride (VII), which is condensed with ethyl cyanacetate (VIII) by means of NaH in glyme yielding ethyl 2-cyano-3-(1-methyl-2-pyrrolyl)-3-oxopropanoate (IX). The reaction of (IX) with aniline (X) in refluxing xylene affords the corresponding anilide (V) already obtained.

1 Walker, G.N. (Novartis AG); alpha-Carbamoyl-pyrrolpropionitriles, process fortheir preparation and pharmaceutical preparations containing them. EP 0143142 .
2 Serradell, M.N.; Castaner, J.; Castaner, R.M.; Prinomide Triethanolamine. Drugs Fut 1987, 12, 8, 773.
中间体序号 中间体编号 品名 CAS号 分子式 供应商 用于合成
(I) 11286 1-Methyl-1H-pyrrole-2-carboxylic acid; 1-Methyl-2-pyrrolecarboxylic acid 6973-60-0 C6H7NO2 详情 详情
(V) 28167 2-cyano-3-(1-methyl-1H-pyrrol-2-yl)-3-oxo-N-phenylpropanamide C15H13N3O2 详情 详情
(VI) 28168 2-[bis(2-hydroxyethyl)amino]-1-ethanol 102-71-6 C6H15NO3 详情 详情
(VII) 28169 1-methyl-1H-pyrrole-2-carbonyl chloride C6H6ClNO 详情 详情
(VIII) 11877 Cyanoacetic acid ethyl ester; Ethyl 2-cyanoacetate; Ethyl cyanoacetate; Ethyl isocyanacetate 105-56-6 C5H7NO2 详情 详情
(IX) 28170 ethyl 2-cyano-3-(1-methyl-1H-pyrrol-2-yl)-3-oxopropanoate C11H12N2O3 详情 详情
(X) 12294 Aniline; Phenylamine 62-53-3 C6H7N 详情 详情
Extended Information