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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1654327Generated: November 2, 2026

Chloroform → dibenzyl 4-[N,N-bis(2-chloroethyl)amino]phenylcarbamoyl-L-glutamate

https://huagongshe.com/reaction/1654327

Reaction equation

Participants

RoleNameHCIDCharge
ReactantChloroformHCID 6212—
ReactantTriethylamineHCID 8471—
ReactantTriphosgeneHCID 94429—
ReactantL-Glutamic acid dibenzyl esterHCID 3037947—
Reactant4-[N,N-bis-(2-chloroethyl)amino]anilinium chlorideHCID 70222082—
Productdibenzyl 4-[N,N-bis(2-chloroethyl)amino]phenylcarbamoyl-L-glutamateHCID 70224102—

Reaction Steps

To a solution of triphosgene (1 g) in chloroform (80 ml) was added at 10° C. 4-[N,N-bis-(2-chloroethyl)amino]anilinium chloride (2.7 g). Whilst keeping the temperature at 10° C., triethylamine (4.15 ml) was added and the mixture was stirred and allowed to warm to ambient temperature for 15 minutes. To this mixture was added in one portion dibenzyl glutamate rosylate and triethylamine (1.7 ml). After 1.5 hours at ambient temperature the mixture was diluted with chloroform (100 ml), washed twice with water, dried and evaporated to dryness. The residue was chromatographed on Merck silica gell Art 9385, eluting with ethyl acetate hexane to give dibenzyl 4[N,N-bis(2-chloroethyl)amino]-phenylcarbamoyl-L-glutamate (2.5 g). m.p. 119°-122° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05405990
Source datasetuspto-grants-1995_04
ORD IDord-de4892b92b354183893d5d5453f19cfc
Source noteuspto-grants-1995_04