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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 867559Generated: October 25, 2026

7-chloro-4,5-dihydro-3-(hydroxymethyl)-5-methyl-6H-imidazo[1,5-a][1,4]benzodiazepin-6-one → 7-chloro-5,6-dihydro-5-methyl-6-oxo-4H-imidazo[1,5-a][1,4]benzodiazepine-3-carboxaldehyde

https://huagongshe.com/reaction/867559

Reaction equation

Participants

RoleNameHCIDCharge
Reactant7-chloro-4,5-dihydro-3-(hydroxymethyl)-5-methyl-6H-imidazo[1,5-a][1,4]benzodiazepin-6-oneHCID 21289952—
CatalystHCID 178418406HCID 178418406—
SolventDichloromethaneHCID 6344—
Product7-chloro-5,6-dihydro-5-methyl-6-oxo-4H-imidazo[1,5-a][1,4]benzodiazepine-3-carboxaldehydeHCID 19851584—

Reaction Steps

18.0 g (64.8 mmol) of 7-chloro-4,5-dihydro-3-hydroxymethyl-5methyl-6H-imidazo[1,5-a][1,4]benzodiazepin-6-one, 75 g of manganese dioxide and 700 ml of methylene chloride are stirred at room temperature for 1.5 hours. The reaction mixture is filtered and the filtrate is evaporated. By recrystallization of the residue from alcohol there is obtained 7-chloro-5,6-dihydro-5-methyl-6-oxo-4H-imidazo[1,5-a][1,4]benzodiazepine-3-carboxaldehyde of melting point 204°-205°.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04775671
Source datasetuspto-grants-1988_10
ORD IDord-73709b47a02c461482d032f18ff8f961
Source noteuspto-grants-1988_10