Methanol → 5-iodo-1-(3-{1-[3-(trifluoromethyl)phenyl]-3-azabicyclo[3.1.0]hex-3-yl}propyl)-2,4(1H,3H)-pyrimidinedione
反応式
[I:1][C:2]1[C:3](=[O:36])[N:4](C(C2C=CC=CC=2)=O)[C:5](=[O:27])[N:6]([CH2:8][CH2:9][CH2:10][N:11]2[CH2:16][CH:15]3[C:13]([C:17]4[CH:22]=[CH:21][CH:20]=[C:19]([C:23]([F:26])([F:25])[F:24])[CH:18]=4)([CH2:14]3)[CH2:12]2)[CH:7]=1.CO>N>[I:1][C:2]1[C:3](=[O:36])[NH:4][C:5](=[O:27])[N:6]([CH2:8][CH2:9][CH2:10][N:11]2[CH2:16][CH:15]3[C:13]([C:17]4[CH:22]=[CH:21][CH:20]=[C:19]([C:23]([F:26])([F:25])[F:24])[CH:18]=4)([CH2:14]3)[CH2:12]2)[CH:7]=1参加物
4
反応物 2
生成物 1
試薬・触媒・溶媒 1
実験手順
(1R,5S/1S,5R) 5-iodo-3-(phenylcarbonyl)-1-(3-{1-[3-(trifluoromethyl)phenyl]-3-azabicyclo[3.1.0]hex-3-yl}propyl)-2,4(1H,3H)-pyrimidinedione (Prep82, 250 mg, 0.410 mmol) was dissolved in 3% ammonia in MeOH, (4 mL, 5.55 mmol). The mixture was stirred at room temperature for 3 hours, the solvent was then evaporated under vacuum and the crude purified by SPE Si (20 g) with Toluene/acetone 80/20 to give a solid that was then loaded through a SCX (5 g) cartridge in order to recover the title compound (168 mg, 0.332 mmol, 81% yield) as a white solid.