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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1065225Generated: October 30, 2026

2-(4-Phenylpiperazin-1-yl)ethan-1-amine → HCID 12941059, compound

https://huagongshe.com/reaction/1065225

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-(4-Phenylpiperazin-1-yl)ethan-1-amineHCID 4742503—
ReactantHCID 12941053HCID 12941053—
SolventTetrahydrofuranHCID 8028—
ProductHCID 12941059HCID 12941059—

Reaction Steps

A mixture of 10.7 g (52.1 mmol) 1-(2-aminoethyl)-4-phenylpiperazine and 13.5 g (54.6 mmol) (R)-4-(2,3-epoxypropoxy)phenylacetic acid, cyanomethyl ester in 125 dry THF was stirred at room temperature for 40 hours. The solvent was removed in vacuo and the residue was triturated with ether to give the crude amide as a white solid. The solid was dissolved in 35 ml. CH2Cl2 and placed on a column of 170 g Woelm basic alumina (grade 3) made up in CHCl2. Elution with 1 liter CH2Cl2 furnished essentially pure material. Crystallization from acetone afforded the end product, m.p. 124°-125°. A second crop, m.p. 121°-123° was obtained from the mother liquors.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04329289
Source datasetuspto-grants-1982_05
ORD IDord-f6460bfec70e47e2a6778088ef557415
Source noteuspto-grants-1982_05