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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1059347Generated: October 31, 2026

1-Benzyl-4-piperidylamine → HCID 178505158, compound

https://huagongshe.com/reaction/1059347

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-Benzyl-4-piperidylamineHCID 415852—
ReactantEthyl (methanesulfonyl)methanimidateHCID 54392285—
SolventDiethyl EtherHCID 3283—
ProductHCID 178505158HCID 17850515839.3%

Reaction Steps

Into a solution of 760 mg of ethyl N-methanesulfonyl-formimidate in diethyl ether (20 ml) was dropped 0.95 g of 4-amino-1-benzylpiperidine at room temperature. After stirring for 2 hours, the crystals thus precipitated were filtered and washed with diethyl ether to thereby give 580 mg of N2-methanesulfonyl-N1-(1-benzylpiperidin-4-yl)formamidine as colorless needles. These crystals were dissolved in 30 ml of methanol and 500 mg of 10% palladium-carbon was added thereto. Then the resulting mixture was stirred in a hydrogen atmosphere under atmospheric pressure for 1 hour followed by filtration through celite. After distilling off the solvent under reduced pressure, the residue was recrystallized from acetone/ethyl acetate to thereby give 310 mg of the title compound as colorless needles.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06518423B1
Source datasetuspto-grants-2003_02
ORD IDord-1b8f01b7c619488cbeede27e00cb2a58
Source noteuspto-grants-2003_02