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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 441484Generated: October 30, 2026

Water → 7-Chloro-5-methoxy-1-methyl-5-phenyl-1,5-dihydro-2H-1,4-benzodiazepin-2-one

https://huagongshe.com/reaction/441484

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantDiethyl EtherHCID 3283—
ReactantSodium hydrideHCID 24758—
Reactant7-Chloro-5-methoxy-1-methyl-4-nitro-5-phenyl-1,3,4,5-tetrahydro-2H-1,4-benzodiazepin-2-oneHCID 3046726—
SolventDimethylformamideHCID 6228—
Product7-Chloro-5-methoxy-1-methyl-5-phenyl-1,5-dihydro-2H-1,4-benzodiazepin-2-oneHCID 304672744.1%

Reaction Conditions

Temperature-30 °C

Reaction Steps

To a solution of sodium hydride (50% suspension in a mineral oil; 200 mg) in dry dimethylformamide (7.5 ml), 7-chloro-5-methoxy-1-methyl-4-nitro-5phenyl-1,3,4,5-tetrahydro-2H-1,4-benzodiazepin-2-one (500 mg) is added under cooling at -30° C. and with stirring, and the resultant mixture is stirred at -10° C. for 30 minutes. The reaction mixture is poured into icy water and shaken with diethyl ether. The organic layer is washed with water, dried over sodium sulfate, and evaporated to remove the solvent. The residue is crystallized from diethyl ether to give 7-chloro-5-methoxy-1-methyl-5-phenyl-1,5-dihydro-2H-1,4-benzodiazepin-2-one (192 mg) as colorless prisms melting at 146.5 to 147° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04041026
Source datasetuspto-grants-1977_08
ORD IDord-1fa956f0e8874173a58464b7d99a8d6b
Source noteuspto-grants-1977_08