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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2202171Generated: November 2, 2026

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

https://huagongshe.com/reaction/2202171

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 numberUS09365529B2
Source datasetuspto-grants-2016_06
ORD IDord-4949243f96b6461ea334b9daeb30b550
Source noteuspto-grants-2016_06