4-(4-Pyrrolidin-1-ylcarbonylbenzyl)-nitrobenzene → 4-[4-(1-Pyrrolidinecarbonyl)benzyl]-phenylamine
反応式
[N:1]1([C:6]([C:8]2[CH:23]=[CH:22][C:11]([CH2:12][C:13]3[CH:18]=[CH:17][C:16]([N+:19]([O-])=O)=[CH:15][CH:14]=3)=[CH:10][CH:9]=2)=[O:7])[CH2:5][CH2:4][CH2:3][CH2:2]1>[Pd].C(O)C>[N:1]1([C:6]([C:8]2[CH:23]=[CH:22][C:11]([CH2:12][C:13]3[CH:18]=[CH:17][C:16]([NH2:19])=[CH:15][CH:14]=3)=[CH:10][CH:9]=2)=[O:7])[CH2:2][CH2:3][CH2:4][CH2:5]1参加物
4
実験手順
A mixture of 4-(4-pyrrolidin-1-ylcarbonylbenzyl)-nitrobenzene (202 mg, 065 mmol), 10% palladium on carbon (110 mg), and ethanol (20 mL) was hydrogenated at 40 psi for 16 hours. The mixture was filtered through a Celite pad, and solvents evaporated to give 4-[4-(1-pyrrolidinecarbonyl)benzyl]-phenylamine as a white solid (187 mg, 99%).