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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1076391Generated: October 25, 2026

Methyl iodide → 7-Chloro-5-(2'-chloro-phenyl)-1,3-dihydro-3-(dimethylaminomethylene)-1-methyl-2H-1,4-benzodiazepin-2-one

https://huagongshe.com/reaction/1076391

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethyl iodideHCID 6328—
ReactantSodium MethoxideHCID 10942334—
Reactant7-Chloro-5-(2'-chloro-phenyl)-1,3-dihydro-3-(dimethylaminomethylene)-2H-1,4-benzodiazepin-2-oneHCID 136353533—
SolventDimethylformamideHCID 6228—
Product7-Chloro-5-(2'-chloro-phenyl)-1,3-dihydro-3-(dimethylaminomethylene)-1-methyl-2H-1,4-benzodiazepin-2-oneHCID 53631932—

Reaction Steps

35.6 gm of a methanolic 30% sodium methylate solution were added dropwise to a solution of 46.5 gm of 7-chloro-5-(2'-chloro-phenyl)-1,3-dihydro-3-(dimethylamino-methylene)-2H-1,4-benzodiazepin-2-one in 300 ml of dry dimethylformamide at room temperature, accompanied by stirring, and the resulting mixture was stirred for 30 minutes more at room temperature and subsequently cooled to +5°C while stirring. Then, while maintaining that temperature by cooling, 58 gm of methyl iodide were added at a slow dropwise rate, again while stirring, and the resulting mixture was stirred for 90 minutes more at +5°C. Thereafter, the yellow precipitate which had formed was collected by vacuum filtration, washed with much water, dried and recrystallized from isopropanol, yielding the compound named in the heading above, which had a melting point of 199°-200°C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS03956492
Source datasetuspto-grants-1976_05
ORD IDord-3fff06df30a54eceb6ab33e163d6bd04
Source noteuspto-grants-1976_05