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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1763251Generated: November 2, 2026

8-chloro-1-methyl-6-phenyl-3,3a,4,6-tetrahydro-5H-imidazo[1,5-a][1,5]benzodiazepin-5-one → 8-Chloro-4,6-dihydro-1-methyl-6-phenyl-5H-imidazo[1,5-a][1,5]benzodiazepin-5-one

https://huagongshe.com/reaction/1763251

Reaction equation

Participants

RoleNameHCIDCharge
Reactant8-chloro-1-methyl-6-phenyl-3,3a,4,6-tetrahydro-5H-imidazo[1,5-a][1,5]benzodiazepin-5-oneHCID 22749550—
CatalystHCID 178418406HCID 178418406—
SolventTolueneHCID 1140—
Product8-Chloro-4,6-dihydro-1-methyl-6-phenyl-5H-imidazo[1,5-a][1,5]benzodiazepin-5-oneHCID 22749546—

Reaction Steps

A mixture of 7.2 g (0.022 moles) of 8-chloro-1-methyl-6-phenyl-3,3a,4,6-tetrahydro-5H-imidazo[1,5-a][1,5]benzodiazepin-5-one, 45 g of activated manganese dioxide and 1.5 l. of toluene was stirred and refluxed for 45 minutes. The manganese dioxide was filtered off and washed well with tetrahydrofuran and methylene chloride. The filtrate was evaporated and the residue was crystallized from ethyl acetate to yield end product with mp 276°-278° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04111931
Source datasetuspto-grants-1978_09
ORD IDord-b2280064700b4bd081c0dd38020f1f99
Source noteuspto-grants-1978_09