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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 223218Generated: October 30, 2026

Thionyl Chloride → HCID 20523292, compound

https://huagongshe.com/reaction/223218

Reaction equation

Participants

RoleNameHCIDCharge
ReactantThionyl ChlorideHCID 24386—
Reactant4,5-dihydro-3-(hydroxymethyl)-5-methyl-6H-imidazo[1,5-a][1,4]benzodiazepin-6-oneHCID 19851602—
SolventBenzeneHCID 241—
ProductHCID 20523292HCID 20523292—

Reaction Steps

6 g (24.6 mmol) of 4,5-dihydro-3-(hydroxymethyl)-5-methyl-6H-imidazo[1,5-a][1,4]benzodiazepin-6-one and 4.45 g of thionyl chloride are heated to boiling under reflux for 2 hours in 50 ml of benzene. The mixture is evaporated to dryness, the residue is taken up in chloroform and washed with 2 N sodium hydroxide. The organic phase is dried over magnesium sulphate and, after removal of the solvent, there is obtained 3-(chloromethyl)-4,5-dihydro-5-methyl-6H-imidazo[1,5-a][1,4]benzodiazepin-6-one of melting point 277°-280°.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04352818
Source datasetuspto-grants-1982_10
ORD IDord-2ba6684a121c4e629236dc557e8417f6
Source noteuspto-grants-1982_10