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【结 构 式】

【分子编号】64995

【品名】3,4,5-tris{[(1,1-dimethylethyl)(dimethyl)silyl]oxy}-6-{[2-(methylamino)-4-nitrophenyl]oxy}tetrahydro-2H-pyran-2-carboxylic acid

【CA登记号】

【 分 子 式 】C31H58N2O9Si3

【 分 子 量 】687.0661

【元素组成】C 54.19% H 8.51% N 4.08% O 20.96% Si 12.26%

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:(III)

The protected glucuronic acid derivative (I) is hydrolyzed under alkaline conditions to furnish (II). The alcoholic hydroxyl groups of (II) are subsequently protected as the silyl ether (III) employing t-butyldimethylsilyl triflate in the presence of DMAP. The carboxyl group of (III) is further converted to the corresponding benzyl ester (IV) by DCC-mediated coupling with benzyl alcohol. Acylation of amine (IV) with phosgene leads to the carbamyl chloride (V). (1,2)

1 Schmidt, F.; Monneret, C.; Prodrug mono therapy: Synthesis and biological evaluation of an etoposide glucuronide-prodrug. Bioorg Med Chem 2003, 11, 10, 2277.
2 Monneret, C.; Schmidt, F. (CNRS (Centre National de la Recherche Scientifique); Institut Curie); Derivs. of etoposide and analogs, and pharmaceutical compsns. containing them. WO 0335661 .
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) 64993 methyl 3,4,5-tris(acetyloxy)-6-{[2-(methylamino)-4-nitrophenyl]oxy}tetrahydro-2H-pyran-2-carboxylate C20H24N2O12 详情 详情
(II) 64994 3,4,5-trihydroxy-6-{[2-(methylamino)-4-nitrophenyl]oxy}tetrahydro-2H-pyran-2-carboxylic acid C13H16N2O9 详情 详情
(III) 64995 3,4,5-tris{[(1,1-dimethylethyl)(dimethyl)silyl]oxy}-6-{[2-(methylamino)-4-nitrophenyl]oxy}tetrahydro-2H-pyran-2-carboxylic acid C31H58N2O9Si3 详情 详情
(IV) 64996 phenylmethyl 3,4,5-tris{[(1,1-dimethylethyl)(dimethyl)silyl]oxy}-6-{[2-(methylamino)-4-nitrophenyl]oxy}tetrahydro-2H-pyran-2-carboxylate C38H64N2O9Si3 详情 详情
(V) 64997 phenylmethyl 6-({2-[(chlorocarbonyl)(methyl)amino]-4-nitrophenyl}oxy)-3,4,5-tris{[(1,1-dimethylethyl)(dimethyl)silyl]oxy}tetrahydro-2H-pyran-2-carboxylate C39H63ClN2O10Si3 详情 详情
Extended Information