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【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