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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 622727Generated: November 1, 2026

Bis(2-chloroethyl)amine → N-[N-(cholest-5-en-3beta-oxycarbonyl)glycyl]bis(2-chloroethyl)amine

https://huagongshe.com/reaction/622727

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBis(2-chloroethyl)amineHCID 9533—
ReactantDicyclohexylcarbodiimideHCID 10868—
ReactantN-(cholest-5-en-3beta-oxycarbonyl)glycineHCID 14168269—
SolventTetrahydrofuranHCID 8028—
ProductN-[N-(cholest-5-en-3beta-oxycarbonyl)glycyl]bis(2-chloroethyl)amineHCID 8674244754.5%

Reaction Steps

To a solution of N-(cholest-5-en-3β-oxycarbonyl)glycine (160.8 mg) in dry tetrahydrofuran (50 ml) was added said bis(2-chloroethyl)amine (85.2 mg) and dicyclohexylcarbodiimide (61.9 mg) at 0° C. under blowing nitrogen gas and the mixture was stirred for 6 hours. After standing overnight (17 hours) at refrigerator, the reaction mixture was filtered and the solvent was evaporated under reduced pressure. The residue was solved in a mixture of chloroform and methanol (50:1) and was subjected to preparation column chromatography (PLC) eluting with a mixture of chloroform and methanol (50:1). The desired parts were gathered, extracted with a mixture of chloroform and methanol (4:1), filtered and concentrated under reduced pressure to give N-[N-(cholest-5-en-3β-oxycarbonyl)glycyl]bis(2-chloroethyl)amine (110 mg).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04772594
Source datasetuspto-grants-1988_09
ORD IDord-bd559e4e847a4eec90e32acf59b57e58
Source noteuspto-grants-1988_09