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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 223228Generated: October 25, 2026

Dimethylformamide → HCID 20523284, compound

https://huagongshe.com/reaction/223228

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDimethylformamideHCID 6228—
ReactantMethyl iodideHCID 6328—
ReactantSodium hydrideHCID 24758—
Reactant7-chloro-4,5-dihydro-3-(hydroxymethyl)-5-methyl-6H-imidazo[1,5-a][1,4]benzodiazepin-6-oneHCID 21289952—
SolventWaterHCID 962—
ProductHCID 20523284HCID 20523284—

Reaction Steps

A mixture of 2.22 g (8 mmol) of 7-chloro-4,5-dihydro-3-(hydroxymethyl)-5-methyl-6H-imidazo[1,5-a][1,4]benzodiazepin-6-one, 0.6 ml (10 mmoL) of methyl iodide and 20 ml of dry dimethylformamide is treated with 0.4 g (9 mmol) of sodium hydride (55 percent oil dispersion, washed with n-hexane) and the mixture is stirred at room temperature for 23 hours. The mixture is poured into 50 ml of water and extracted four times with methylene chloride. The methylene chloride solution is dried over magnesium sulphate and evaporated. The crude product is chromatographed on silica gel using methylene chloride containing 1% of methanol for the elution. By subsequent recrystallization from ethyl acetate/n-hexane there is obtained 7-chloro-4,5-dihydro-3-(methoxymethyl)-5-methyl-6H-imidazo[1,5-a][1,4]benzodiazepin-6-one of melting point 143°-144°.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04352818
Source datasetuspto-grants-1982_10
ORD IDord-361118361581463ab1f9ff1c9894006f
Source noteuspto-grants-1982_10