Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 586372Generated: October 29, 2026

Thionyl Chloride → 2-Chloromethyl-3-(1-propyl)-imidazolo[1,2-a]pyridine

https://huagongshe.com/reaction/586372

Reaction equation

Participants

RoleNameHCIDCharge
ReactantThionyl ChlorideHCID 24386—
Reactant2-Hydroxymethyl-3-(1-propyl)-imidazolo[1,2-a]pyridineHCID 22335047—
SolventDichloromethaneHCID 6344—
SolventEthyl AcetateHCID 8857—
Product2-Chloromethyl-3-(1-propyl)-imidazolo[1,2-a]pyridineHCID 22335060—

Reaction Steps

Thionyl chloride (125 mg, 1.06 mmol) is added to a solution of 2-hydroxymethyl-3-(1-propyl)-imidazolo[1,2-a]pyridine (100 mg, 0.53 mmol) in CH2Cl2 (3 mL) at 0° C. under nitrogen with magnetic stirring. After 1 hour, the reaction is diluted with EtOAc (20 mL), washed with saturated aqueous NaHCO3 (10 mL), water (10 mL) and brine (10 mL). The solution is then dried over anhydrous sodium sulfate, filtered and evaporated at reduced pressure to obtain 2-chloromethyl-3-(1-propyl)-imidazolo[1,2-a]pyridine as a colorless oil. TLC (10% MeOH/CH2Cl2) Rf=0.60. Step 5. Preparation of 3-{1-[(3-propylimidazo[1,2-a]pyridin-2-yl)methyl]-1H-imidazol-2-yl}benzonitrile

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06936617B2
Source datasetuspto-grants-2005_08
ORD IDord-8ad0518c2cf24898b0c7b4a219712732
Source noteuspto-grants-2005_08