HuagongsheHuagongshe Chemistry Print Report · For research reference only
Tetrahydrofuran → N-[2-(Diethylamino)ethyl]-4-(2-pyridinyl)-1-piperazine carboxamide, hydrochloride
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Tetrahydrofuran | HCID 8028 | — |
| Reactant | 1-(2-Pyridyl)piperazine | HCID 94459 | — |
| Reactant | N-[2-(Hexahydro-1H-azepin-1-yl)ethyl]-4-phenyl-1-piperazinecarboxamide hydrochloride | HCID 22163783 | — |
| Solvent | Hydrochloric Acid | HCID 313 | — |
| Product | N-[2-(Diethylamino)ethyl]-4-(2-pyridinyl)-1-piperazine carboxamide, hydrochloride | HCID 131716591 | — |
Reaction Steps
This compound was prepared according to the procedure used to synthesize the compound of Example 9. A mixture of 5.0 g (0.03 mole) of 1',1'-carbonyldiimidazole, 3.6 g (0.03 mole) of unsym-diethylethylenediamine, and 5.0 g (0.03 mole) of 1-(2-pyridinyl)piperazine in a total of 200 ml of tetrahydrofuran gave an oil as residue. The hydrochloride was formed in ethereal hydrogen chloride and the collected solid was recrystallized from methanol-ethyl ether to yield 7.3 g (63%) of title compound as a white solid, m.p. 183°-185° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04960776 |
| Source dataset | uspto-grants-1990_10 |
| ORD ID | ord-8e283edddd6747b487b40281c7b0e63b |
| Source note | uspto-grants-1990_10 |