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【结 构 式】 
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【分子编号】60761 【品名】3-(1H-imidazol-1-ylcarbonyl)-4-methoxybenzenesulfonamide 【CA登记号】 |
【 分 子 式 】C11H11N3O4S 【 分 子 量 】281.29216 【元素组成】C 46.97% H 3.94% N 14.94% O 22.75% S 11.4% |
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：(V)The reaction of imidazole (I) with phosgene (II) in hot benzene gives carbonyldiimidazole (III), which is condensed with 5-sulfamoyl-2-methoxybenzoic acid (IV) in THF yielding 1-(5-sulfamoyl-2-methoxybenzoyl)imidazole (V). Finally this compound is condensed with 1-methyl-2-aminomethylpyrrolidine (VI) in THF at room temperature
| 【1】 (Société d'Estude Scientifiques et Industrielles de I'lle-de-France.); BE 658250; CA 801043; CH 468377; DE 1595915; DE 1795723; FR 1472025; GB 1088531; JP 6706913; JP 6923496; NL 6500326; US 3342826; ZA 6406127 |
| 【2】 CH 468377 . |
| 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) | 10255 | Imidazole; 1H-Imidazole | 288-32-4 | C3H4N2 | 详情 | 详情 |
| (III) | 11353 | 1,1'-Carbonyldiimidazole; Di(1H-imidazol-1-yl)methanone; N,N-Carbonyldiimidazole; 1,1'-Carbonylbis(1H-imidazole) | 530-62-1 | C7H6N4O | 详情 | 详情 |
| (IV) | 21355 | 5-(aminosulfonyl)-2-methoxybenzoic acid; 2-methoxy-5-sulfamoylbenzoic acid | 22117-85-7 | C8H9NO5S | 详情 | 详情 |
| (V) | 60761 | 3-(1H-imidazol-1-ylcarbonyl)-4-methoxybenzenesulfonamide | C11H11N3O4S | 详情 | 详情 | |
| (VI) | 60759 | (1-methyl-2-pyrrolidinyl)methylamine; (1-methyl-2-pyrrolidinyl)methanamine | C6H14N2 | 详情 | 详情 |
Extended Information