HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 517501Generated: October 30, 2026
Hydrochloric Acid → methyl (R)-3-amino-2-(4-methanesulphonylpiperazin-1-yl)propanoate hydrochloride
https://huagongshe.com/reaction/517501
Participants
| Role | Name | HCID | Charge |
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| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | methyl (R)-3-tert-butoxycarbonylamino-2-(4-methanesulphonyl-piperazin-1-yl)propanoate | HCID 67056910 | — |
| Solvent | Methanol | HCID 887 | — |
| Solvent | Isopropanol | HCID 3776 | — |
| Product | methyl (R)-3-amino-2-(4-methanesulphonylpiperazin-1-yl)propanoate hydrochloride | HCID 67056954 | 97% |
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 3.8 g (10.4 mmol) of methyl (R)-3-tert-butoxycarbonylamino-2-(4-methanesulphonylpiperazin-1-yl)propanoate in 50 ml of methanol. The reaction medium is stirred at 40° C. for 3 h, concentrated under vacuum then taken up in diethyl ether. The product precipitates, is filtered, rinsed with diethyl ether then dried under vacuum. 3 g (97%) of methyl (R)-3-amino-2-(4-methanesulphonylpiperazin-1-yl)propanoate hydrochloride are obtained in the form of a beige solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09115102B2 |
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| Source dataset | uspto-grants-2015_08 |
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| ORD ID | ord-a30cd320a53749c29211a019bf456ace |
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| Source note | uspto-grants-2015_08 |
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