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【结 构 式】

【分子编号】63444

【品名】7-nitro-1H-indole-2-carboxylic acid

【CA登记号】

【 分 子 式 】C9H6N2O4

【 分 子 量 】206.15772

【元素组成】C 52.44% H 2.93% N 13.59% O 31.04%

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:(VIII)

5-Nitrobenzofuran-2-carboxylic acid (I) is coupled to 4-nitrophenol (II) in the presence of EDC to produce the p-nitrophenyl ester (III). Subsequent acylation of the duocarmycin derivative (IV) with active ester (III) leads to amide (V). Cyclopropane ring opening in (V) with HCl in DMF furnishes the chloromethyl derivative (VI). The nitro group of (VI) is then reduced by catalytic hydrogenation, yielding amine (VII). Acylation of (VII) with 7-nitroindole-2-carboxylic acid (VIII) affords the corresponding amide (IX)

1 McGee, D.P.C.; Saunders, O.L.; Martichonok, V.; Wu, G.; Ng, H.P.; Li, Z.; Yarranton, G.T. (Medarex, Inc.); Cytotoxic agents. US 2003050331; WO 0296910 .
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) 63365 5-nitro-1-benzofuran-2-carboxylic acid 10242-12-3 C9H5NO5 详情 详情
(II) 11236 4-Nitrophenol; p-Nitrophenol 100-02-7 C6H5NO3 详情 详情
(III) 63440 4-nitrophenyl 5-nitro-1-benzofuran-2-carboxylate C15H8N2O7 详情 详情
(IV) 38365 methyl (3bR,4aS)-2-methyl-8-oxo-1,4,4a,5,6,8-hexahydrocyclopropa[c]pyrrolo[3,2-e]indole-3-carboxylate C14H14N2O3 详情 详情
(V) 63441 methyl 2-methyl-6-[(5-nitro-1-benzofuran-2-yl)carbonyl]-8-oxo-1,4,4a,5,6,8-hexahydrocyclopropa[c]pyrrolo[3,2-e]indole-3-carboxylate C23H17N3O7 详情 详情
(VI) 63442 methyl 8-(chloromethyl)-4-hydroxy-2-methyl-6-[(5-nitro-1-benzofuran-2-yl)carbonyl]-3,6,7,8-tetrahydropyrrolo[3,2-e]indole-1-carboxylate C23H18ClN3O7 详情 详情
(VII) 63443 methyl 6-[(5-amino-1-benzofuran-2-yl)carbonyl]-8-(chloromethyl)-4-hydroxy-2-methyl-3,6,7,8-tetrahydropyrrolo[3,2-e]indole-1-carboxylate C23H20ClN3O5 详情 详情
(VIII) 63444 7-nitro-1H-indole-2-carboxylic acid C9H6N2O4 详情 详情
(IX) 63445 methyl 8-(chloromethyl)-4-hydroxy-2-methyl-6-[(5-{[(7-nitro-1H-indol-2-yl)carbonyl]amino}-1-benzofuran-2-yl)carbonyl]-3,6,7,8-tetrahydropyrrolo[3,2-e]indole-1-carboxylate C32H24ClN5O8 详情 详情
Extended Information