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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 266700Generated: October 25, 2026

Piperidine → N-phenyl beta-(8-hydroxy-5-quinolyl)-alpha-cyanoacrylamide

https://huagongshe.com/reaction/266700

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPiperidineHCID 8082—
ReactantAcetamide, 2-cyano-N-phenyl-HCID 69296—
Reactant8-Hydroxyquinoline-5-carbaldehydeHCID 275363—
SolventEthanolHCID 702—
ProductN-phenyl beta-(8-hydroxy-5-quinolyl)-alpha-cyanoacrylamideHCID 5451708875%

Reaction Steps

A solution of 8-hydroxy-5-quinolinecarboxaldehyde (1.732 g, 0.010 mol), N-phenyl cyanoacetamide (1.602 g, 0.010 mol) and piperidine (0.255 g, 0.003 mol) in absolute ethanol (50 ml) was heated for 3 h at reflux. The reaction mixture was chilled to about 10°-15° C., the precipitate filtered, the residue washed with ice-cooled ethanol and dried under vacuum. Almost pure title compound was obtained in about 75% yield (2.365 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05652250
Source datasetuspto-grants-1997_07
ORD IDord-ca1bb5d3581b40c3be74bfd295d6c6c7
Source noteuspto-grants-1997_07