[4-(6-Chloro-5-nitro-pyrimidin-4-ylamino)-phenyl]-acetic acid ethyl ester → [4-(5-Amino-6-chloro-pyrimidin-4-ylamino)-phenyl]acetic acid ethyl ester
反応式
[CH2:1]([O:3][C:4](=[O:23])[CH2:5][C:6]1[CH:11]=[CH:10][C:9]([NH:12][C:13]2[C:18]([N+:19]([O-])=O)=[C:17]([Cl:22])[N:16]=[CH:15][N:14]=2)=[CH:8][CH:7]=1)[CH3:2]>C1COCC1.[Ni]>[CH2:1]([O:3][C:4](=[O:23])[CH2:5][C:6]1[CH:7]=[CH:8][C:9]([NH:12][C:13]2[C:18]([NH2:19])=[C:17]([Cl:22])[N:16]=[CH:15][N:14]=2)=[CH:10][CH:11]=1)[CH3:2]参加物
4
実験手順
A mixture of [4-(6-chloro-5-nitro-pyrimidin-4-ylamino)-phenyl]-acetic acid ethyl ester (0.400 g, 1.19 mmol) and Raney Ni (˜0.100 g) in THF (10 mL) is stirred for 20.5 h at rt, under a hydrogen atmosphere. The reaction mixture is filtered through a pad of celite and concentrated. Purification of the residue by silica gel column chromatography (Hexane/EtOAc, 70:30) provides the title compound as a yellow solid: ES-MS: 307.1 [M+H]+; single peak at tR=3.81 min (System 1); Rf=0.06 (Hexane/EtOAc, 70:30).