Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 586374Generated: October 27, 2026

2-(3-fluorophenyl)-1H-imidazole → 6-chloro-2-{[2-(3-fluorophenyl)-1H-imidazol-1-yl]methyl}-3-propylimidazo[1,2-a]pyridine

https://huagongshe.com/reaction/586374

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-(3-fluorophenyl)-1H-imidazoleHCID 316816—
ReactantDichloromethane methanolHCID 21226129—
Reactant2-Chloromethyl-6-chloro-3-(1-propyl)-imidazolo[1,2-a]pyridineHCID 22335107—
SolventEthyl AcetateHCID 8857—
SolventDimethylacetamideHCID 31374—
Product6-chloro-2-{[2-(3-fluorophenyl)-1H-imidazol-1-yl]methyl}-3-propylimidazo[1,2-a]pyridineHCID 22335084—

Reaction Conditions

Temperature60 °C

Reaction Steps

Kt-BuO (0.69 mL of 1 M in THF, 0.69 mmol) is added to a solution of 3-fluoro-(1H-imidazol-2-yl)benzene (88 mg, 0.58 mmol) in anhydrous DMA (1 mL). After 15 minutes, 2-chloromethyl-6-chloro-3-(1-propyl)-imidazolo[1,2-a]pyridine (140 mg, 0.58 mmol) is added and the reaction mixture is stirred and heated at 60° C. for 15 minutes. The reaction mixture is diluted with EtOAc (10 mL), washed with water (3 mL), brine (3 mL), dried over Na2SO4, filtered and evaporated at reduced pressure to obtain a yellow solid. Sequential chromatography on silica gel eluting with EtOAc and then 5%MeOH/CH2Cl2 provides 6-chloro-2-{[2-(3-fluoropheny)-1H-imidazol-1-yl]methyl}-3-propylimidazo[1,2-a]pyridine as a cream-colored yellow solid. TLC (10% MeOH/CH2Cl2) Rf=0.35.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06936617B2
Source datasetuspto-grants-2005_08
ORD IDord-8d638e36cfbd4aaab052ecb27541dd34
Source noteuspto-grants-2005_08