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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 5727Generated: October 25, 2026

1-Phenylpiperazine → 1-(N-Benzyloxycarbonyltyrosyl)-4-phenylpiperazine

https://huagongshe.com/reaction/5727

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-PhenylpiperazineHCID 7096—
ReactantDicyclohexylcarbodiimideHCID 10868—
ReactantN-benzyloxycarbonyl-l-tyrosineHCID 712438—
SolventDichloromethaneHCID 6344—
Product1-(N-Benzyloxycarbonyltyrosyl)-4-phenylpiperazineHCID 5446385658.6%

Reaction Steps

12.3 g of N-benzyloxycarbonyltyrosine and 6.6 g of N-phenylpiperazine were dissolved in 150 ml of methylene chloride, and to the solution was added 8.4 g of DCC, and the mixture was stirred at a room temperature for 5 hours. Precipitated insoluble matter was filtered off and the filtrate was concentrated under a reduced pressure, and resulting residue was applied to a silica gel column and eluted with hexane/ethyl acetate (1:1 to 1:2) to obtain 10.5 g of the title compound in a colorless amorphous form.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05245034
Source datasetuspto-grants-1993_09
ORD IDord-6fb0cb4113fb499eb4dfc30867774f34
Source noteuspto-grants-1993_09