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【结 构 式】

【分子编号】14095

【品名】4,5-Dibromo-2-thiophenecarbonyl chloride

【CA登记号】

【 分 子 式 】C5HBr2ClOS

【 分 子 量 】304.38904

【元素组成】C 19.73% H 0.33% Br 52.5% Cl 11.65% O 5.26% S 10.53%

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:(II)

A new synthesis of tenidap sodium has been described: The reaction of 4,5-dibromothiophene-2-carboxylic acid (I) with hot SOCl2 gives the corresponding acyl chloride (II), which is condensed with 5-chloro-2-oxo-2,3-dihydro-1H-indole-1-carboxamide (III) by means of 4-(dimethylamino)pyridine (DMAP) in DMF, yielding 5-chloro-3-[(4,5-dibromothien-2-yl)hydroxymethylene]-2-oxo-2,3-dihydro-1H-indole-1-carboxamide (IV). Finally, this compound is debrominated by hydrogenation with H2 over Pd/BaSO4 in methanol.

1 Schulte, G.R.; Ehrgott, F.J. (Pfizer Inc.); 3-Aroyl-2-oxindole-1-carboxamides. EP 0421749; JP 1991151380; US 5059693 .
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) 14094 4,5-Dibromo-2-thiophenecarboxylic acid; 4,5-Dibromothiophene-2-carboxylic acid 7311-68-4 C5H2Br2O2S 详情 详情
(II) 14095 4,5-Dibromo-2-thiophenecarbonyl chloride C5HBr2ClOS 详情 详情
(III) 14096 5-Chloro-2-oxo-1-indolinecarboxamide C9H7ClN2O2 详情 详情
(IV) 14097 5-Chloro-3-[(Z)-(4,5-dibromo-2-thienyl)(hydroxy)methylidene]-2-oxo-1H-indole-1(2H)-carboxamide C14H7Br2ClN2O3S 详情 详情
Extended Information