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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1242832Generated: October 25, 2026

tert-Butyl piperazine-1-carboxylate → Methyl 2-Carbobenzyloxyamino-3-(4-tert-butoxycarbonylpiperazin-1-yl)propionate

https://huagongshe.com/reaction/1242832

Reaction equation

Participants

RoleNameHCIDCharge
Reactanttert-Butyl piperazine-1-carboxylateHCID 143452—
ReactantZ-Dehydro-Ala-OMeHCID 3525700—
SolventAcetonitrile methanolHCID 21959252—
ProductMethyl 2-Carbobenzyloxyamino-3-(4-tert-butoxycarbonylpiperazin-1-yl)propionateHCID 21940471—

Reaction Steps

To N-carbobenzyloxydehydroalanine methyl ester (2.0 g, 8.4 mmol) was added 4-tert-butoxycarbonylpiperazine (1.56 g, 1.0 eq), ferric chloride (0.220 g, 0.2 eq) in a 6:1 mixture of acetonitrile/methanol. The reaction mixture was stirred at room temperature for 2 days. The reaction mixture was evaporated under reduced pressure. EtOAc was added and the organic layer washed with a soldium sulfate solution. Upon removal of the solvent under reduced pressure, the crude material was purified by column chromatography (silica gel; CH2Cl2:MeOH 4:1) to afford the title compound.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07115768B2
Source datasetuspto-grants-2006_10
ORD IDord-6213b1c896734390adf615de7d5e2173
Source noteuspto-grants-2006_10