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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1966102Generated: October 30, 2026

Hydrochloric Acid → Methyl (S)-3-amino-2-(4-methanesulfonylpiperazin-1-yl)propanoate dihydrochloride

https://huagongshe.com/reaction/1966102

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
Reactantmethyl (S)-3-tert-butoxycarbonylamino-2-(4-methanesulfonylpiperazin-1-yl)propanoateHCID 67056930—
SolventMethanolHCID 887—
SolventDiethyl EtherHCID 3283—
SolventIsopropanolHCID 3776—
ProductMethyl (S)-3-amino-2-(4-methanesulfonylpiperazin-1-yl)propanoate dihydrochlorideHCID 86675013—

Reaction Conditions

Temperature40 °C

Reaction Steps

A solution of 4 g (11 mmol) of methyl (S)-3-tert-butoxycarbonylamino-2-(4-methanesulfonylpiperazin-1-yl)propanoate (prepared as described in example 2.4) in 40 ml of methanol and 20 ml of a solution of hydrochloric acid in isopropanol, having a concentration of 5 or 6M, is stirred at 40° C. for 18 h and then concentrated under vacuum. The residue obtained is taken up in 200 ml of diethyl ether, filtered, and then dried under vacuum, 3.5 g (94%) of methyl (S)-3-amino-2-(4-methanesulfonylpiperazin-1-yl)propanoate dihydrochloride are obtained in the form of a beige solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08420632B2
Source datasetuspto-grants-2013_04
ORD IDord-62f808213a4142ab8a5bb0c2f77033c7
Source noteuspto-grants-2013_04