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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 354763Generated: October 29, 2026

Ammonia → 7-amino-6,8,9-trichloro-1,3-dihydro-5-(o-fluorophenyl)-1,3,3-trimethyl-2H-1,4-benzodiazepin-2-one

https://huagongshe.com/reaction/354763

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAmmoniaHCID 222—
ReactantDichloromethaneHCID 6344—
ReactantN-chlorosuccinamideHCID 15238416—
Reactant7-amino-9-chloro-5-(o-fluorophenyl)-1,3-dihydro-1,3,3-trimethyl-2H-1,4-benzodiazepin-2-oneHCID 20506143—
Product7-amino-6,8,9-trichloro-1,3-dihydro-5-(o-fluorophenyl)-1,3,3-trimethyl-2H-1,4-benzodiazepin-2-oneHCID 20506196—

Reaction Steps

4.75 g (0.014 mol) of 7-amino-9-chloro-5-(o-fluorophenyl)-1,3-dihydro-1,3,3-trimethyl-2H-1,4-benzodiazepin-2-one are dissolved in 100 ml of dry methylene chloride and treated with 4.2 g of N-chlorosuccinamide. The reaction mixture is heated at reflux for 40 hours, treated with 25 percent aqueous ammonia and extracted several times with methylene chloride. After drying and evaporating the organic phase, the residue is chromatographed on 250 g of silica gel with methylene chloride/ethyl acetate (20:1) as the elution agent. There is obtained 7-amino-6,8,9-trichloro-1,3-dihydro-5-(o-fluorophenyl)-1,3,3-trimethyl-2H-1,4-benzodiazepin-2-one of melting point 165°-166° (ether/n-hexane).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04377522
Source datasetuspto-grants-1983_03
ORD IDord-4dbd35921bbf4ba2bc446592765819a2
Source noteuspto-grants-1983_03