Cl.[Cl:2][C:3]1[CH:4]=[C:5]([CH2:10][CH2:11][C@H:12]([NH2:14])[CH3:13])[CH:6]=[CH:7][C:8]=1Cl.[F:15][C:16]([F:25])([F:24])C1C=CC=CC=1O>>[ClH:2].[F:15][C:16]([F:25])([F:24])[C:3]1[CH:4]=[C:5]([CH2:10][CH2:11][C@H:12]([NH2:14])[CH3:13])[CH:6]=[CH:7][CH:8]=1Intermediate 5 (55 mg, 0.25 mmol, 88% yield) was prepared as a white powder following the procedure described for Intermediate 4 by replacing 2,6-dichlorophenol with 2-trifluromethylphenol. LC-MS (ESI) 218.1 (M+H), RT=1.60 min (Method B).
Wird geladen…