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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 354747Generated: October 25, 2026

Chlorine → 7-amino-6-chloro-5-(o-chlorophenyl)-1,3-dihydro-1,3,3-trimethyl-2H-1,4-benzodiazepin-2-one

https://huagongshe.com/reaction/354747

Reaction equation

Participants

RoleNameHCIDCharge
ReactantChlorineHCID 24526—
Reactant7-amino-5-(o-chlorophenyl)-1,3-dihydro-1,3,3-trimethyl-2H-1,4-benzodiazepin-2-oneHCID 20506178—
SolventAcetic AcidHCID 176—
Product7-amino-6-chloro-5-(o-chlorophenyl)-1,3-dihydro-1,3,3-trimethyl-2H-1,4-benzodiazepin-2-oneHCID 20506150—

Reaction Steps

17 g (0.052 mol) of 7-amino-5-(o-chlorophenyl)-1,3-dihydro-1,3,3-trimethyl-2H-1,4-benzodiazepin-2-one in 100 ml of glacial acetic acid are treated slowly with a solution of 4 g of chlorine gas in 50 ml of glacial acetic acid. The reaction mixture is stirred at room temperature, evaporated after 60 minutes and the residue is treated with aqueous ammonia and methylene chloride. After extracting the aqueous phase with methylene chloride, the organic extract is dried and evaporated. The crude product is purified by chromatography on 600 g of silica gel with methylene chloride and methylene chloride/ethyl acetate (5:1) as the elution agent. From ethyl acetate/ether/n-hexane there is obtained 7-amino-6-chloro-5-(o-chlorophenyl)-1,3-dihydro-1,3,3-trimethyl-2H-1,4-benzodiazepin-2-one of melting point 195°-196°.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04377522
Source datasetuspto-grants-1983_03
ORD IDord-126f32c10a284008a3bc107ff869f7ff
Source noteuspto-grants-1983_03