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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1087822Generated: October 25, 2026

Tetrahydrofuran → N-[2-(Diethylamino)ethyl]-4-(2-pyridinyl)-1-piperazine carboxamide, hydrochloride

https://huagongshe.com/reaction/1087822

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTetrahydrofuranHCID 8028—
Reactant1-(2-Pyridyl)piperazineHCID 94459—
ReactantN-[2-(Hexahydro-1H-azepin-1-yl)ethyl]-4-phenyl-1-piperazinecarboxamide hydrochlorideHCID 22163783—
SolventHydrochloric AcidHCID 313—
ProductN-[2-(Diethylamino)ethyl]-4-(2-pyridinyl)-1-piperazine carboxamide, hydrochlorideHCID 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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04960776
Source datasetuspto-grants-1990_10
ORD IDord-8e283edddd6747b487b40281c7b0e63b
Source noteuspto-grants-1990_10