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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 224368Generated: October 25, 2026

Ammonia → 3-fluoro-5-o-fluorophenyl-7-nitro-2,3-dihydro-1H-1,4-benzodiazepin-2-one

https://huagongshe.com/reaction/224368

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAmmoniaHCID 222—
ReactantHexamethylenetetramineHCID 4101—
Reactant2-Amino-2'-fluoro-5-nitrobenzophenoneHCID 67657—
Reactant2-(alpha-Bromo-alpha-fluoroacetamido)-5-nitro-2'-fluorobenzophenoneHCID 23332640—
Reactantalpha-Bromo-alpha-fluoroacetyl bromideHCID 23332663—
SolventEthanolHCID 702—
Product3-fluoro-5-o-fluorophenyl-7-nitro-2,3-dihydro-1H-1,4-benzodiazepin-2-oneHCID 23332560—

Reaction Steps

NH3 is passed into a refluxing solution of 1.48 g. of hexamethylenetetramine in 30 ml. of ethanol; 3.83 g. of 2-(α-bromo-α-fluoroacetamido)-5-nitro-2'-fluorobenzophenone, obtainable from 2-amino-5-nitro-2'-fluorobenzophenone and α-bromo-α-fluoroacetyl bromide, are added over 2 hours. The mixture is then heated under reflux for 3 hours more and is evaporated. The resulting 2-(α-amino-α-fluoroacetamido)-5-nitro-2'-fluorobenzophenone is treated with 15 ml. of toluene and 20 mg. of p-tolunesulfonic acid and is heated under reflux for 1 hour. Working up in the customary manner gives 3-fluoro-5-o-fluorophenyl-7-nitro-2,3-dihydro-1H-1,4-benzodiazepin-2-one.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04232016
Source datasetuspto-grants-1980_11
ORD IDord-5b5b4ec6a18646e5ada4fff703b054be
Source noteuspto-grants-1980_11