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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 517500Generated: October 26, 2026

Water → methyl (R)-3-tert-butoxycarbonylamino-2-(4-methanesulphonyl-piperazin-1-yl)propanoate

https://huagongshe.com/reaction/517500

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
Reactantn,n-Bis(2-chloroethyl)methanesulfonamideHCID 245092—
Reactant(R)-Methyl 2-amino-3-((tert-butoxycarbonyl)amino)propanoate hydrochlorideHCID 51358429—
SolventDiisopropylethylamineHCID 81531—
Productmethyl (R)-3-tert-butoxycarbonylamino-2-(4-methanesulphonyl-piperazin-1-yl)propanoateHCID 6705691044.1%

Reaction Steps

A solution of 6 g (23.6 mmol) of methyl (R)-2-amino-3-tert-butoxycarbonylaminopropanoate hydrochloride and 5.2 g (23.6 mmol) of N,N-bis(2-chloroethyl)methanesulphonamide in 80 ml of N,N-diisopropylethylamine is heated at 125° C. with vigorous stirring for 18 h. After addition of water, the product is extracted with ethyl acetate. The organic phases are combined, washed with water, dried over magnesium sulphate, filtered and concentrated under vacuum. The crude product obtained is purified by chromatography over silica gel eluted with a 5/5 heptane/ethyl acetate mixture. 3.8 g (44%) of methyl (R)-3-tert-butoxycarbonylamino-2-(4-methanesulphonylpiperazin-1-yl)propanoate are obtained in the form of a white solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09115102B2
Source datasetuspto-grants-2015_08
ORD IDord-9bb9523c700248b9a01547df2c48ab39
Source noteuspto-grants-2015_08