【结 构 式】 |
【分子编号】30733 【品名】4-amino-2-chloro-5-(1H-1,2,3,4-tetraazol-5-yl)benzenesulfonamide 【CA登记号】 |
【 分 子 式 】C7H7ClN6O2S 【 分 子 量 】274.69052 【元素组成】C 30.61% H 2.57% Cl 12.91% N 30.59% O 11.65% S 11.67% |
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 synthetic procedure for azosemide has been reported: The condensation of 2-formylthiophene (I) with 2-chloro-4-amino-5-(5-tetrazolyl)benzenesulfonamide (II) by means of polyphosphoric acid (PPA) in DMSO gives the corresponding Schiff base (III), which is reduced with KBH4 in the same solvent.
【1】 Baetz, F.; Lauer, K. (Boehringer Ingelheim GmbH); Process for the production of 5-(4'-chloro-5'-sulfamoyl-2'-thenylamino)phenyltetrazole. DE 3034664; JP 57081485 . |
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) | 30732 | 2-thiophenecarbaldehyde; Thiophene-2-carboxaldehyde | 98-03-3 | C5H4OS | 详情 | 详情 |
(II) | 30733 | 4-amino-2-chloro-5-(1H-1,2,3,4-tetraazol-5-yl)benzenesulfonamide | C7H7ClN6O2S | 详情 | 详情 | |
(III) | 30734 | 2-chloro-5-(1H-1,2,3,4-tetraazol-5-yl)-4-[[(E)-2-thienylmethylidene]amino]benzenesulfonamide | C12H9ClN6O2S2 | 详情 | 详情 |
Extended Information