Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 472143Generated: October 30, 2026

HCID 71115295, compound → Methyl (S)-3-tert-butoxycarbonylamino-2-piperazin-1-ylpropanoate

https://huagongshe.com/reaction/472143

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHCID 71115295HCID 71115295—
SolventEthanolHCID 702—
ProductMethyl (S)-3-tert-butoxycarbonylamino-2-piperazin-1-ylpropanoateHCID 86675027—

Reaction Steps

(21 mmol) of methyl(S)-2-(4-benzylpiperazin-1-yl)-3-tert-butoxycarbonylaminopropanoate (prepared as described in example 17.4) in 120 ml of ethanol, degassed beforehand under a nitrogen stream. The reaction medium is then placed under a hydrogen atmospheric pressure for 24 h and then filtered through celite and thoroughly rinsed with dichloromethane. After concentration under vacuum, 6.1 g (100%) of methyl (S)-3-tert-butoxycarbonylamino-2-piperazin-1-ylpropanoate are obtained.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08633196B2
Source datasetuspto-grants-2014_01
ORD IDord-98521336825a40faa03a61adc1650cd6
Source noteuspto-grants-2014_01