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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1966098Generated: October 31, 2026

Hydrochloric Acid → methyl (S)-3-amino-2-(4-methanesulphonylpiperazin-1-yl)propanoate hydrochloride

https://huagongshe.com/reaction/1966098

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
Reactantmethyl (S)-3-tert-butoxycarbonylamino-2-(4-methanesulfonylpiperazin-1-yl)propanoateHCID 67056930—
SolventMethanolHCID 887—
SolventIsopropanolHCID 3776—
Productmethyl (S)-3-amino-2-(4-methanesulphonylpiperazin-1-yl)propanoate hydrochlorideHCID 67057002100%

Reaction Conditions

Temperature40 °C

Reaction Steps

15 ml of a solution of hydrochloric acid in isopropanol, having a concentration of 5-6N are added dropwise to a solution of 2.7 g (7.4 mmol) of methyl (S)-3-tert-butoxycarbonylamino-2-(4-methanesulfonylpiperazin-1-yl)propanoate in 30 ml of methanol. The reaction medium is stirred at 40° C. for 2 h, concentrated under vacuum, and then taken up in 20 ml of methanol and 150 ml of diethyl ether. The product precipitates, and is filtered off under vacuum, rinsed with diethyl ether and then dried under vacuum. 2.3 g (100%) of methyl (S)-3-amino-2-(4-methanesulfonylpiperazin-1-yl)propanoate hydrochloride are obtained in the form of a white solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08420632B2
Source datasetuspto-grants-2013_04
ORD IDord-59f2be691522485b8677e74f5953b047
Source noteuspto-grants-2013_04