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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 500114Generated: October 31, 2026

2-Chloro-3-(4-methoxyphenyl)propanal → 6-(4-Fluorophenyl)-3-(4-methoxybenzyl)imidazo[1,2-a]pyrimidine

https://huagongshe.com/reaction/500114

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-Chloro-3-(4-methoxyphenyl)propanalHCID 12102756—
Reactant5-(4-Fluorophenyl)pyrimidin-2-amineHCID 12946647—
Solvent2-Methyl-2-butanolHCID 6405—
Product6-(4-Fluorophenyl)-3-(4-methoxybenzyl)imidazo[1,2-a]pyrimidineHCID 25145512—

Reaction Conditions

Temperature130 °C

Reaction Steps

A mixture of 5-(4-fluorophenyl)pyrimidin-2-amine (50 mg, 0.3 mmol), 2-chloro-3-(4-methoxyphenyl)propanal (52 mg, 0.26 mmol) in tert-amyl alcohol (1.0 mL) in a sealed reaction vial was heated at 130° C. for 3 hours. After cooling, the mixture was purified by preparative HPLC to afford the desired product. LCMS: (M+H)=334.0.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07767675B2
Source datasetuspto-grants-2010_08
ORD IDord-cc7561f2aeec4985a6270737d3ff10a8
Source noteuspto-grants-2010_08