HuagongsheHuagongshe Chemistry Print Report · For research reference only
2-(4-Phenylpiperazin-1-yl)ethan-1-amine → HCID 12941059, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 2-(4-Phenylpiperazin-1-yl)ethan-1-amine | HCID 4742503 | — |
| Reactant | HCID 12941053 | HCID 12941053 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 12941059 | HCID 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
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04285873 |
| Source dataset | uspto-grants-1981_08 |
| ORD ID | ord-c7ded445533f4d96b2b7fc16b7464876 |
| Source note | uspto-grants-1981_08 |