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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2202194Generated: October 27, 2026

Hydrochloric Acid → methyl (S)-3-amino-2-(4-ethylpiperazin-1-yl)propanoate trihydrochloride

https://huagongshe.com/reaction/2202194

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
Reactantmethyl (S)-3-tert-butoxycarbonylamino-2-(4-ethylpiperazin-1-yl)propanoateHCID 86667916—
SolventMethanolHCID 887—
Productmethyl (S)-3-amino-2-(4-ethylpiperazin-1-yl)propanoate trihydrochlorideHCID 8667502454%

Reaction Conditions

Temperature40 °C

Reaction Steps

2.5 g (7.9 mmol) of methyl (S)-3-tert-butoxycarbonylamino-2-(4-ethylpiperazin-1-yl)propanoate are placed in 20 ml of methanol and 10 ml of isopropanolic hydrochloric acid having a concentration of 5-6N. The reaction medium is heated at 40° C. for 3 h and then evaporated to dryness. The residue is taken up in 50 ml of ethanol, stirred for 1 h at ambient temperature and then filtered. 1.4 g (54%) of methyl (S)-3-amino-2-(4-ethylpiperazin-1-yl)propanoate trihydrochloride are obtained in the form of a beige solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09365529B2
Source datasetuspto-grants-2016_06
ORD IDord-ed495ec9f6054b0b8caab73ccf5cc383
Source noteuspto-grants-2016_06