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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1679291Generated: October 30, 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/1679291

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 numberUS04080323
Source datasetuspto-grants-1978_03
ORD IDord-f58a05b10c8f423a8d4be6e40273c1f5
Source noteuspto-grants-1978_03