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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 894975Generated: October 30, 2026

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

https://huagongshe.com/reaction/894975

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 numberUS04285873
Source datasetuspto-grants-1981_08
ORD IDord-c7ded445533f4d96b2b7fc16b7464876
Source noteuspto-grants-1981_08