3-Bromo-7-(trifluoromethyl)imidazo[1,2-a]pyrimidine → 3,2-Difluoro-5-(7-trifluoromethylimidazo[1,2-a]pyrimidin-3-yl)biphenyl-2-carbonitrile
反応式
Br[C:2]1[N:6]2[CH:7]=[CH:8][C:9]([C:11]([F:14])([F:13])[F:12])=[N:10][C:5]2=[N:4][CH:3]=1.CC1(C)COB([C:22]2[CH:23]=[CH:24][C:25]([F:37])=[C:26]([C:28]3[C:29]([C:35]#[N:36])=[C:30]([F:34])[CH:31]=[CH:32][CH:33]=3)[CH:27]=2)OC1>>[F:34][C:30]1[CH:31]=[CH:32][CH:33]=[C:28]([C:26]2[CH:27]=[C:22]([C:2]3[N:6]4[CH:7]=[CH:8][C:9]([C:11]([F:14])([F:13])[F:12])=[N:10][C:5]4=[N:4][CH:3]=3)[CH:23]=[CH:24][C:25]=2[F:37])[C:29]=1[C:35]#[N:36]参加物
3
実験手順
3-Bromo-7-trifluoromethylimidazo[1,2-α]pyrimidine was coupled with 5′-(5,5-dimethyl-[1,3,2]dioxaborinan-2-yl)-3,2′-difluorobiphenyl-2-carbonitrile as described in Example 1 to give 3,2′-difluoro-5′-(7-trifluoromethylimidazo[1,2-α]pyrimidin-3-yl)biphenyl-2-carbonitrile as an off-white solid: δH (360 MHz, CDCl3) 7.31 (2H, dd, J 7 and 3), 7.43-7.49 (2H, m), 7.64-7.75 (3H, m), 8.10 (1H, s), 9.04 (1H, d, J 7); m/z (ES+) 401 (M++H).
出典と根拠
- ORDレコード
- ord-6b488bb4ac95437d9f6856eb1815586c
- 出典データセット
- uspto-grants-2005_05
- 特許番号
- US06900215B2
反応ノート
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