Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 478237Generated: October 29, 2026

3'-(4,4,5,5-Tetramethyl-[1,3,2]dioxaborolan-2-yl)biphenyl-2-carbonitrile → 3'-(7-Difluoromethylimidazo[1,2-a]pyrimidin-3-yl)biphenyl-2-carbonitrile

https://huagongshe.com/reaction/478237

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3'-(4,4,5,5-Tetramethyl-[1,3,2]dioxaborolan-2-yl)biphenyl-2-carbonitrileHCID 11243655—
Reactant3-Bromo-7-difluoromethylimidazo[1,2-a]pyrimidineHCID 18001286—
Product3'-(7-Difluoromethylimidazo[1,2-a]pyrimidin-3-yl)biphenyl-2-carbonitrileHCID 994617558%

Reaction Steps

3-Bromo-7-difluoromethylimidazo[1,2-a]pyrimidine (248 mg, 1.00 mmol) was coupled with 3′-(4,4,5,5-tetramethyl-[1,3,2]dioxaborolan-2-yl)biphenyl-2-carbonitrile as described in Example 1 to give 3′-(7-difluoromethylimidazo[1,2-a]pyrimidin-3-yl)biphenyl-2-carbonitrile (201 mg, 58%) as a yellow powder: δH (400 MHz, CDCl3) 6.67 (1H, t, J 55) 7.29 (1H, d, J 7), 7.52 (1H, td, J 9 and 1), 7.58-7.74 (5H, m), 7.87 (2H, m), 8.01 (1H, s), 9.12 (1H, d, J 7); m/z (ES+) 347 (M++H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06642229B2
Source datasetuspto-grants-2003_11
ORD IDord-762390e6400b4e0588debce229997ed1
Source noteuspto-grants-2003_11