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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1796066Generated: November 4, 2026

Imidazo[1,2-a]pyrimidine, 3-(tributylstannyl)-7-(trifluoromethyl)- → HCID 9858693, compound

https://huagongshe.com/reaction/1796066

Reaction equation

Participants

RoleNameHCIDCharge
ReactantImidazo[1,2-a]pyrimidine, 3-(tributylstannyl)-7-(trifluoromethyl)-HCID 11294484—
Reactant2-Bromo-6-(1H-imidazol-1-yl)pyridineHCID 22180782—
ProductHCID 9858693HCID 985869315.9%

Reaction Steps

2-Bromo-6-(1H-imidazol-1-yl)pyridine (0.18 g, 0.8 mmol) was coupled to 3-tributylstannyl-7-trifluoromethylimidazo[1,2-α]pyrimidine (0.9 mmol) by the method of Example 1. Purification by chromatography on silica gel eluting with dichloromethane on a gradient of methanol (0-10%) and trituration with ethyl acetate gave 3-[6-(1H-imidazol-1-yl)pyridin-2-yl]-7-trifluoromethylimidazo[1,2-α]pyrimidine (42 mg) as an off-white solid: δH (400 MHz, CDCl3) 7.30 (1H, s), 7.35 (1H, d, J 8), 7.43 (1H, d, J 7), 7.65 (1H, s), 7.79 (1H, d, J 8), 8.00 (1H, dd, J 8 and 8), 8.38 (1H, s), 8.59 (1H, s), 10.24 (1H, d, J 7); m/z (ES+) 331 (M++H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07030128B2
Source datasetuspto-grants-2006_04
ORD IDord-ee0f4a2593f542b1a390b1774c42b1cd
Source noteuspto-grants-2006_04