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【结 构 式】

【分子编号】56425

【品名】tert-butyl 2-{[(6-amino-1H-indol-2-yl)carbonyl]amino}ethylcarbamate

【CA登记号】

【 分 子 式 】C16H22N4O3

【 分 子 量 】318.37584

【元素组成】C 60.36% H 6.96% N 17.6% O 15.08%

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)

Reaction of methyl 6-nitroindole-2-carboxylate (I) with ethylenediamine (II) in hot DMF gives amino amide (III). After protection of (III) as the N-Boc derivative (IV), catalytic hydrogenation of its nitro group affords amine (V). Indole-2,5-dicarboxylic (VI) is activated as the bis-pentafluorophenyl ester (VII) by treatment with pentafluorophenyl trifluoroacetate. Subsequent coupling between the bis-pentafluorophenyl ester (VII) and amino indole (V) furnishes diamide (VIII). Removal of the N-Boc groups using trifluoroacetic acid in the presence of anisole produces diamine (IX).

1 Roberts, C.; et al.; Discovery af a new class of broad-spectrum antifungal compounds that target the minor groove of DNA. 28th Natl Med Chem Symp (June 8 2002, San Diego) 2002, Abst 67.
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) 56422 methyl 6-nitro-1H-indole-2-carboxylate C10H8N2O4 详情 详情
(II) 14754 ethylenediamine;1,2-Diaminoethane;ethane-1,2-diamine;1,2-Ethanediamine 107-15-3 C2H8N2 详情 详情
(III) 56423 N-(2-aminoethyl)-6-nitro-1H-indole-2-carboxamide C11H12N4O3 详情 详情
(IV) 56424 tert-butyl 2-{[(6-nitro-1H-indol-2-yl)carbonyl]amino}ethylcarbamate C16H20N4O5 详情 详情
(V) 56425 tert-butyl 2-{[(6-amino-1H-indol-2-yl)carbonyl]amino}ethylcarbamate C16H22N4O3 详情 详情
(VI) 56426 1H-indole-2,5-dicarboxylic acid C10H7NO4 详情 详情
(VII) 56427 bis(2,3,4,5,6-pentafluorophenyl) 1H-indole-2,5-dicarboxylate C22H5F10NO4 详情 详情
(VIII) 56428 tert-butyl 2-[({6-[({2-[({2-[({2-[(tert-butoxycarbonyl)amino]ethyl}amino)carbonyl]-1H-indol-6-yl}amino)carbonyl]-1H-indol-5-yl}carbonyl)amino]-1H-indol-2-yl}carbonyl)amino]ethylcarbamate C42H47N9O8 详情 详情
(IX) 56429 N~2~,N~5~-bis(2-{[(2-aminoethyl)amino]carbonyl}-1H-indol-6-yl)-1H-indole-2,5-dicarboxamide C32H31N9O4 详情 详情
Extended Information