5'-Bromo-2',6-difluorobiphenyl-2-carbonitrile → 6,2'-Difluoro-5'-(8-fluoro-7-trifluoromethylimidazo[1,2-alpha]pyridin-3-yl)-biphenyl-2-carbonitrile

HRID 1180317Notes

Reaction equation

HRID 1180317 reaction equation
[F:1][C:2]1[C:3]2[N:4]([CH:12]=[CH:13][N:14]=2)[CH:5]=[CH:6][C:7]=1[C:8]([F:11])([F:10])[F:9].Br[C:16]1[CH:17]=[CH:18][C:19]([F:31])=[C:20]([C:22]2[C:23]([C:29]#[N:30])=[CH:24][CH:25]=[CH:26][C:27]=2[F:28])[CH:21]=1>>[F:28][C:27]1[CH:26]=[CH:25][CH:24]=[C:23]([C:29]#[N:30])[C:22]=1[C:20]1[CH:21]=[C:16]([C:12]2[N:4]3[CH:5]=[CH:6][C:7]([C:8]([F:9])([F:10])[F:11])=[C:2]([F:1])[C:3]3=[N:14][CH:13]=2)[CH:17]=[CH:18][C:19]=1[F:31]

Participants

3

Procedure

8-Fluoro-7-trifluoromethylimidazo[1,2-α]pyridine (102 mg, 0.5 mmol) and 5′-bromo-6,2′-difluorobiphenyl-2-carbonitrile (221 mg, 0.75 mmol) were coupled following the procedure given in Example 6 to afford 6,2′-difluoro-5′-(8-fluoro-7-trifluoromethylimidazo[1,2-α]pyridin-3-yl)-biphenyl-2-carbonitrile (65 mg, 31%) as a white solid: δH (360 MHz, CDCl3) 6.99 (1H, dd, J 7 and 6), 7.41-7.51 (2H, m), 7.54-7.60 (1H, m), 7.62-7.69 (3H, m), 7.87 (1H, s), 8.33 (1H, d, J 7); m/z (ES+) 418 (100%, [MH]+).

Sources & evidence

ORD record
ord-c272cee5b12c471687a0735e4dc65f85
Source dataset
uspto-grants-2007_10
Patent number
US07279580B2

Reaction notes

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