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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 848537Generated: October 30, 2026

Water → Urea, N,N-dimethyl-N(sup 1)-(5-(2-fluorophenyl)-2,3-dihydro-1-methyl-2-oxo-1H-1,4-benzodiazepin-7-yl)-

https://huagongshe.com/reaction/848537

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantDimethylcarbamoyl ChlorideHCID 6598—
ReactantPotassium CarbonateHCID 11430—
Reactant7-AminoflunitrazepamHCID 92294—
SolventDichloromethaneHCID 6344—
ProductUrea, N,N-dimethyl-N(sup 1)-(5-(2-fluorophenyl)-2,3-dihydro-1-methyl-2-oxo-1H-1,4-benzodiazepin-7-yl)-HCID 3058275—

Reaction Conditions

Temperature20 °C

Reaction Steps

4.2 g (0.015 M) of 7-amino-5-(o-fluorophenyl)-1,3-dihydro-1-methyl-2H-1,4-benzodiazepin-2-one are suspended in 60 ml of absolute methylene chloride, treated with 2.1 g of powdered potassium carbonate and 1.6 ml of dimethylcarbamoyl chloride and stirred at 20° C. for 14 days. The mixture is then poured on to a mixture of ice and water, extracted with methylene chloride and the organic phase is washed 2-3 times with water, dried with sodium sulphate, filtered and concentrated. The residue is purified on a 200 g silica gel column using ethyl acetate as the eluting agent and crystallised from ethanol/petroleum ether. There is obtained 3-[5-(o-fluorophenyl)-2,3-dihydro-1-methyl-2-oxo-1H-1,4-benzodiazepin-7-yl]-1,1-dimethylurea which crystallises with 0.5 mol of ethanol and melts at 97° C. with decomposition.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04296031
Source datasetuspto-grants-1981_10
ORD IDord-6135fdd6afee431099dfb98441864571
Source noteuspto-grants-1981_10