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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1413784Generated: October 31, 2026

Triethylamine → HCID 20562330, compound

https://huagongshe.com/reaction/1413784

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
Reactant2-Chloroethyl isocyanateHCID 16035—
Reactant7-AminoflunitrazepamHCID 92294—
SolventTetrahydrofuranHCID 8028—
ProductHCID 20562330HCID 20562330—

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 heated at reflux for 3 hours in 80 ml of absolute tetrahydrofuran with 3.5 ml of chloroethylisocyanate and a catalytic amount of triethylamine. The mixture is left to stand at room temperature overnight. The solution is concentrated on a steam-bath and the residue is crystallised from ethyl acetate. There is obtained 1-(2-chloroethyl)-3-[5-(o-fluorophenyl)-2,3-dihydro-1-methyl-2-oxo-1H-1,4-benzodiazepin-7-yl]urea which melts at 240° C. with decomposition.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04251443
Source datasetuspto-grants-1981_02
ORD IDord-fc12079818424668ace7239f8675b011
Source noteuspto-grants-1981_02