tert-butyl N-(2-methyl-4-oxobutan-2-yl)carbamate → Tert-butyl {3-[2-(1-hydroxycyclohexyl)phenylamino]-1,1-dimethylpropyl}carbamate
反応式
[NH2:1][C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][C:3]=1[C:8]1([OH:14])[CH2:13][CH2:12][CH2:11][CH2:10][CH2:9]1.[C:15]([O:19][C:20](=[O:28])[NH:21][C:22]([CH3:27])([CH3:26])[CH2:23][CH:24]=O)([CH3:18])([CH3:17])[CH3:16]>CCCCCC.CCOC(C)=O>[C:15]([O:19][C:20](=[O:28])[NH:21][C:22]([CH3:27])([CH3:26])[CH2:23][CH2:24][NH:1][C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][C:3]=1[C:8]1([OH:14])[CH2:13][CH2:12][CH2:11][CH2:10][CH2:9]1)([CH3:18])([CH3:17])[CH3:16]参加物
4
実験手順
The product is prepared analogously to intermediate product 1b starting from 1-(2-aminophenyl)cyclohexanol and tert-butyl(1,1-dimethyl-3-oxopropyl)carbamate. After column chromatography (silica gel, hexane/EtOAc 7:1) the product is obtained as a colorless oil. Yield: 2.65 g (66%); Rf=0.50 (silica gel, hexane/EtOAc 4:1).