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【结 构 式】

【分子编号】33748

【品名】[(1S)-1-(bromomethyl)-5-[[tert-butyl(dimethyl)silyl]oxy]-7-methyl-1,6-dihydropyrrolo[3,2-e]indol-3(2H)-yl](5,6,7-trimethoxy-1H-indol-2-yl)methanone

【CA登记号】

【 分 子 式 】C30H38BrN3O5Si

【 分 子 量 】628.63844

【元素组成】C 57.32% H 6.09% Br 12.71% N 6.68% O 12.73% Si 4.47%

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:(X)

Decarboxylation of (IX) in refluxing bromobenzene yielded (X), which was converted to the 3-bromoindole (XI) by reaction with N-bromosuccinimide in the presence of silicagel. Desilylation of (XI) with tetrabutylammonium fluoride gave phenol (XII), and further intramolecular cyclization of (XII) with simultaneous amide hydrolysis by treatment with NaOMe produced the cyclopropyl cyclohexadienone (XIII). Finally, the 4-methoxycinnamoyl group was introduced in (XIII) by condensation with the 4-nitrophenyl ester (XIV) in the presence of NaH at -20 C.

1 Okabe, M.; Tamaoki, T.; Saito, H.; Okamoto, A.; Amishiro, N.; Murakata, C.; Synthesis and antitumor activity of duocarmycin derivatives: Modification of segment-A of A-ring pyrrole compounds. J Med Chem 1999, 42, 15, 2946-60.
中间体序号 中间体编号 品名 CAS号 分子式 供应商 用于合成
(IX) 33747 (8S)-8-(bromomethyl)-4-[[tert-butyl(dimethyl)silyl]oxy]-2-methyl-6-[(5,6,7-trimethoxy-1H-indol-2-yl)carbonyl]-3,6,7,8-tetrahydropyrrolo[3,2-e]indole-1-carboxylic acid C31H38BrN3O7Si 详情 详情
(X) 33748 [(1S)-1-(bromomethyl)-5-[[tert-butyl(dimethyl)silyl]oxy]-7-methyl-1,6-dihydropyrrolo[3,2-e]indol-3(2H)-yl](5,6,7-trimethoxy-1H-indol-2-yl)methanone C30H38BrN3O5Si 详情 详情
(XI) 33749 [(1S)-8-bromo-1-(bromomethyl)-5-[[tert-butyl(dimethyl)silyl]oxy]-7-methyl-1,6-dihydropyrrolo[3,2-e]indol-3(2H)-yl](5,6,7-trimethoxy-1H-indol-2-yl)methanone C30H37Br2N3O5Si 详情 详情
(XII) 33750 [(1S)-8-bromo-1-(bromomethyl)-5-hydroxy-7-methyl-1,6-dihydropyrrolo[3,2-e]indol-3(2H)-yl](5,6,7-trimethoxy-1H-indol-2-yl)methanone C24H23Br2N3O5 详情 详情
(XIII) 33751 (3bR,4aS)-3-bromo-2-methyl-4,4a,5,6-tetrahydrocyclopropa[c]pyrrolo[3,2-e]indol-8(1H)-one C12H11BrN2O 详情 详情
(XIV) 33752 4-nitrophenyl (E)-3-(4-methoxyphenyl)-2-propenoate C16H13NO5 详情 详情
Extended Information