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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2183942Generated: November 1, 2026

3-Bromo-7-(trifluoromethyl)imidazo[1,2-a]pyrimidine → 3-[2-Fluoro-3-(pyridin-3-yl)phenyl]-7-trifluoromethylimidazo[1,2-alpha]pyrimidine

https://huagongshe.com/reaction/2183942

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3-Bromo-7-(trifluoromethyl)imidazo[1,2-a]pyrimidineHCID 11391462—
Reactant2-Fluoro-3-(pyridin-3-yl)phenylboronic acidHCID 22285316—
Product3-[2-Fluoro-3-(pyridin-3-yl)phenyl]-7-trifluoromethylimidazo[1,2-alpha]pyrimidineHCID 10133007—

Reaction Steps

3-Bromo-7-trifluoromethylimidazo[1,2-α]pyrimidine was coupled with 2-fluoro-3-(pyridin-3-yl)benzeneboronic acid as described in Example 1 to give 3-[2-fluoro-3-(pyridin-3-yl)phenyl]-7-trifluoromethylimidazo[1,2-α]pyrimidine as an off-white solid. Bis-hydrochloride salt (from ethyl acetate/ethanol): δH (360 MHz, DMSO) 7.62 (2H, dd, J 7 and 7), 7.85-7.96 (3H, m), 8.36 (1H, s), 8.58 (1H, d, J 8), 8.86 (1H, dd, J 5 and 1), 9.14 (1H, s), 9.33 (1H, dd, J 7 and 3); m/z (ES+) 359 (M++H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06900215B2
Source datasetuspto-grants-2005_05
ORD IDord-5befec7aef094b118dd30199f8f6fce8
Source noteuspto-grants-2005_05