【结 构 式】 |
【分子编号】35478 【品名】N-[(1S)-3-diazo-1-(dodecylsulfanyl)-2-oxopropyl]acetamide 【CA登记号】 |
【 分 子 式 】C17H31N3O2S 【 分 子 量 】341.51816 【元素组成】C 59.79% H 9.15% N 12.3% O 9.37% S 9.39% |
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 alkylation of N-acetyl-L-cysteine (I) with dodecyl bromide (II) by means of ammonia in methanol gives N-acetyl-S-dodecyl-L-cysteine (III), which is treated with isobutyl chloroformate and N-methylmorpholine (NMM) in THF yielding the mixed anhydride (IV). The reaction of (IV) with diazomethane in ethyl ether affords the diazoketone (V), which is finally treated with HCl in ethyl acetate.
【1】 Narla, R.K.; Uckun, F.M.; Perry, D.A. (Parker Hughes Institute); Alkyl ketones as potent anti-cancer agents. WO 0000469 . |
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) | 35475 | (2S)-2-(acetamido)-2-sulfanylethanoic acid | C4H7NO3S | 详情 | 详情 | |
(II) | 24062 | 1-bromododecane | 143-15-7 | C12H25Br | 详情 | 详情 |
(III) | 35476 | (2S)-2-(acetamido)-2-(dodecylsulfanyl)ethanoic acid | C16H31NO3S | 详情 | 详情 | |
(IV) | 35477 | C21H39NO5S | 详情 | 详情 | ||
(V) | 35478 | N-[(1S)-3-diazo-1-(dodecylsulfanyl)-2-oxopropyl]acetamide | C17H31N3O2S | 详情 | 详情 |
Extended Information