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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2183968Generated: October 26, 2026

3-bromo-7-(trifluoromethyl)imidazo[1,2-a]pyrimidine → 5,2-Difluoro-5-(7-trifluoromethylimidazo[1,2-a]pyrimidin-3-yl)biphenyl-2-carbonitrile

https://huagongshe.com/reaction/2183968

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3-bromo-7-(trifluoromethyl)imidazo[1,2-a]pyrimidineHCID 11391462—
Reactant5'-(5,5-Dimethyl-[1,3,2]dioxaborinan-2-yl)-5,2'-difluorobiphenyl-2-carbonitrileHCID 11688443—
Product5,2-Difluoro-5-(7-trifluoromethylimidazo[1,2-a]pyrimidin-3-yl)biphenyl-2-carbonitrileHCID 10200975—

Reaction Steps

3-Bromo-7-trifluoromethylimidazo[1,2-α]pyrimidine was coupled with 5′-(5,5-dimethyl-[1,3,2]dioxaborinan-2-yl)-5,2′-difluorobiphenyl-2-carbonitrile as described in Example 1 to give 5,2′-difluoro-5′-(7-trifluoromethylimidazo[1,2-α]pyrimidin-3-yl)biphenyl-2-carbonitrile as an off-white solid: δH (360 MHz, CDCl3) 7.25-7.31 (2H, m), 7.44-7.50 (1H, m), 7.67 (1H, ddd, J 9, 5 and 2), 7.67 (1H, s), 7.69 (1H, s), 7.88 (1H, dd, J 9 and 6), 8.11 (1H, s), 9.05 (1H, d, J 7); m/z (ES+) 401 (M++H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06900215B2
Source datasetuspto-grants-2005_05
ORD IDord-6571c13d6b324ac5838d76f434c67188
Source noteuspto-grants-2005_05