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【结 构 式】

【分子编号】57895

【品名】N-[(2R)-2-(3,4-bis{[tert-butyl(dimethyl)silyl]oxy}phenyl)-2-hydroxyethyl]-4-(4-{[tert-butyl(dimethyl)silyl]oxy}phenyl)butanamide

【CA登记号】

【 分 子 式 】C36H63NO5Si3

【 分 子 量 】674.15646

【元素组成】C 64.14% H 9.42% N 2.08% O 11.87% Si 12.5%

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:(VII)

The enantioselective condensation of 3,4-bis(tert-butyldimethylsilyloxy)benzaldehyde (I) with nitromethane (II), catalyzed by the chiral Zn ligand complex (III) in THF gives the (R)-2-nitroethanol derivative (IV), which is reduced with H2 over Pd/C in methanol to yield the 2-aminoethanol derivative (V). The condensation of (V) with 4-[4-(tert-butyldimethylsilyloxy)phenyl]butyric acid (VI) by means of diphenyl chlorophosphate and DIEA in dichloromethane affords the corresponding amide (VII), which is reduced by conventional methods to the protected hydroxyamine (VIII). Finally, this compound is desilylated as usual to furnish the target tetrahydroxyamine derivative.

1 Ito, H.; Bremeyer, N.; Trost, B.M.; Yeh, V.S.C.; Effect of ligand structure on the zinc-catalyzed Henry reaction. Asymmetric syntheses of (-)-denopamine and (-)-arbutamine. Org Lett 2002, 4, 16, 2621.
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) 55602 3,4-bis{[tert-butyl(dimethyl)silyl]oxy}benzaldehyde C19H34O3Si2 详情 详情
(II) 39563 nitromethane 75-52-5 CH3NO2 详情 详情
(III) 57893   C64H60O3Zn2 详情 详情
(IV) 55605 (1R)-1-(3,4-bis{[tert-butyl(dimethyl)silyl]oxy}phenyl)-2-nitro-1-ethanol C20H37NO5Si2 详情 详情
(V) 55606 (1R)-2-amino-1-(3,4-bis{[tert-butyl(dimethyl)silyl]oxy}phenyl)-1-ethanol C20H39NO3Si2 详情 详情
(VI) 57894 4-(4-{[tert-butyl(dimethyl)silyl]oxy}phenyl)butanoic acid C16H26O3Si 详情 详情
(VII) 57895 N-[(2R)-2-(3,4-bis{[tert-butyl(dimethyl)silyl]oxy}phenyl)-2-hydroxyethyl]-4-(4-{[tert-butyl(dimethyl)silyl]oxy}phenyl)butanamide C36H63NO5Si3 详情 详情
(VIII) 57896 (1R)-1-(3,4-bis{[tert-butyl(dimethyl)silyl]oxy}phenyl)-2-{[4-(4-{[tert-butyl(dimethyl)silyl]oxy}phenyl)butyl]amino}-1-ethanol C36H65NO4Si3 详情 详情
Extended Information