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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1190794Generated: October 31, 2026

Thionyl Chloride → HCID 15294730, compound

https://huagongshe.com/reaction/1190794

Reaction equation

Participants

RoleNameHCIDCharge
ReactantThionyl ChlorideHCID 24386—
ReactantHCID 69292992HCID 69292992—
SolventChloroformHCID 6212—
ProductHCID 15294730HCID 15294730—

Reaction Steps

A solution of 1.74 mmol of N-tert-Butyl-4-(5,6,7,8-tetrahydro-imidazo[1,5-a]pyridin-8-yl)-benzamide hydrochloride and 1.4 ml of thionyl chloride in 30 ml of chloroform is stirred under reflux for 7 hours. The reaction mixture is cooled to room temperature and evaporated. The residue is taken up in dichloromethane and mixed with saturated aqueous sodium bicarbonate solution. The organic phase is separated off and the aqueous phase is extracted with dichloromethane (2×). The combined organic phases are dried with sodium sulphate and evaporated. Following flash chromatography (SiO2 60F) of the residue, the resulting solid is stirred in 1:1 diethyl ether/tert-butyl methyl ether, filtered and dried. The title compound is obtained as a cream-colored solid. Rf=0.37 (toluene:methanol=85:15); Rt=4.88

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08680079B2
Source datasetuspto-grants-2014_03
ORD IDord-28e2c927390348018e35798d50e42ba6
Source noteuspto-grants-2014_03