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【结 构 式】

【分子编号】42322

【品名】tert-butyl (2S)-1-[(4-[2-[(benzhydrylamino)carbothioyl]hydrazino]-3-nitrophenyl)sulfonyl]-2-pyrrolidinecarboxylate

【CA登记号】

【 分 子 式 】C29H33N5O6S2

【 分 子 量 】611.74312

【元素组成】C 56.94% H 5.44% N 11.45% O 15.69% S 10.48%

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:(VI)

Condensation of 4-chloro-3-nitrobenzenesulfonyl chloride (VII) with L-proline tert-butyl ester (VIII) yielded sulfonamide (IX). Displacement of the chloro group of (IX) with hydrazine hydrate furnished the aryl hydrazine (X), which was reacted with benzhydryl isothiocyanate (XI) to produce the thiosemicarbazide (XII). After acid cleavage of the tert-butyl ester of (XII), the resulting carboxylic acid (XIII) was activated with isobutyl chloroformate and then coupled with triamine (VI) to furnish the title amide.

1 Ritchie, T.J.; Hallett, A.; Dziadulewicz, E.K.; et al.; 1-(2-Nitrophenyl)thiosemicarbazides: A novel class of potent, orally active non-peptide antagonist for the bradykinin B2 receptor. J Med Chem 2000, 43, 5, 769.
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) 42318 4-chloro-3-nitrobenzenesulfonyl chloride 97-08-5 C6H3Cl2NO4S 详情 详情
(II) 19832 tert-butyl (2S)-2-pyrrolidinecarboxylate C9H17NO2 详情 详情
(III) 42319 tert-butyl (2S)-1-[(4-chloro-3-nitrophenyl)sulfonyl]-2-pyrrolidinecarboxylate C15H19ClN2O6S 详情 详情
(IV) 42320 tert-butyl (2S)-1-[(4-hydrazino-3-nitrophenyl)sulfonyl]-2-pyrrolidinecarboxylate C15H22N4O6S 详情 详情
(V) 42321 1-[isothiocyanato(phenyl)methyl]benzene; benzhydryl isothiocyanate 3550-21-8 C14H11NS 详情 详情
(VI) 42322 tert-butyl (2S)-1-[(4-[2-[(benzhydrylamino)carbothioyl]hydrazino]-3-nitrophenyl)sulfonyl]-2-pyrrolidinecarboxylate C29H33N5O6S2 详情 详情
(VII) 42323 (2S)-1-[(4-[2-[(benzhydrylamino)carbothioyl]hydrazino]-3-nitrophenyl)sulfonyl]-2-pyrrolidinecarboxylic acid C25H25N5O6S2 详情 详情
(VIII) 42317 N-(2-aminoethyl)-N-[2-(dimethylamino)ethyl]-N-methylamine; N(1)-(2-aminoethyl)-N(1),N(2),N(2)-trimethyl-1,2-ethanediamine C7H19N3 详情 详情
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