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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 478252Generated: October 25, 2026

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

https://huagongshe.com/reaction/478252

Reaction equation

Participants

RoleNameHCIDCharge
ReactantImidazo[1,2-a]pyrimidine, 3-(tributylstannyl)-7-(trifluoromethyl)-HCID 11294484—
Reactant1-(3'-bromobiphenyl-2-yl)-1H-[1,2,4]triazoleHCID 18001279—
SolventMethanolHCID 887—
SolventDichloromethaneHCID 6344—
Product3-[2'-([1,2,4]Triazol-1-yl)biphenyl-3-yl]-7-trifluoromethylimidazo[1,2-a]pyrimidineHCID 10179468—

Reaction Steps

1-(3′-Bromobiphenyl-2-yl)-1H-[1,2,4]triazole (91 mg, 0.30 mmol) was coupled to 3-tributylstannyl-7-trifluoromethylimidazo[1,2-a]pyrimidine (0.25 mmol) by the method of Example 32. The product was obtained by preparative thin-layer chromatography on silica gel with 3% methanol in dichloromethane as eluent followed by high performance liquid chromatography to give 3-[2′-([1,2,4]triazol-1-yl)biphenyl-3-yl]-7-trifluoromethylimidazo[1,2-a]pyrimidine as a yellow solid: δH (400 MHz, CDCl3) 8.57 (1H, d, J 7), 7.95-8.11 (3H, m), 7.48-7.66 (7H, m), 7.35 (1H, J 8), 7.27 (1H, m); m/z (ES+) 407 (M++H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06642229B2
Source datasetuspto-grants-2003_11
ORD IDord-afe692c0c5d5474c8490b62b0f7422a0
Source noteuspto-grants-2003_11