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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 478249Generated: October 26, 2026

Imidazo[1,2-a]pyrimidine, 3-(tributylstannyl)-7-(trifluoromethyl)- → 3-[3-([1,2,4]Triazol-1-yl)-phenyl]-7-trifluoromethylimidazo[1,2-a]pyrimidine

https://huagongshe.com/reaction/478249

Reaction equation

Participants

RoleNameHCIDCharge
ReactantImidazo[1,2-a]pyrimidine, 3-(tributylstannyl)-7-(trifluoromethyl)-HCID 11294484—
Reactant1-(3-bromophenyl)-1H-1,2,4-triazoleHCID 22329498—
Product3-[3-([1,2,4]Triazol-1-yl)-phenyl]-7-trifluoromethylimidazo[1,2-a]pyrimidineHCID 9880574—

Reaction Steps

1-(3-Bromophenyl)-1H-[1,2,4]triazole (1.7 g, 7.6 mmol) was coupled to 3-tributylstannyl-7-trifluoromethylimidazo[1,2-a]pyrimidine (3.8 mmol) by the method of Example 32. Purification by chromatography on silica gel eluting with dichloromethane on a gradient of methanol (1-3%), then crystallisation from toluene/isohexane, gave 3-[3-([1,2,4]triazol-1-yl)-phenyl]-7-trifluoromethylimidazo[1,2-a]pyrimidine as an off-white solid: δH (400 MHz, DMSO) 9.43 (1H, d, J 7), 9.41 (1H, s), 8.38 (1H, s), 8.30 (1H, s), 8.26-8.28 (1H, m), 7.97-8.00 (1H, m), 7.76-7.81 (2H, m), 7.56 (1H, d, J 7); m/z (ES+) 331 (M++H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06642229B2
Source datasetuspto-grants-2003_11
ORD IDord-c8aaa1f10b2d427fb80d06ff7999e7e2
Source noteuspto-grants-2003_11