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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1846619Generated: November 3, 2026

1-(Piperidin-4-yl)ethan-1-ol → HCID 67340994, compound

https://huagongshe.com/reaction/1846619

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-(Piperidin-4-yl)ethan-1-olHCID 338321—
ReactantHCID 86676282HCID 86676282—
SolventAcetonitrileHCID 6342—
ProductHCID 67340994HCID 6734099465%

Reaction Steps

A mixture of 0.200 g (1.55 mmol) of 1-piperidin-4-yl-ethanol and 0.200 g (0.663 mmol) of 3-chloro-N-(2,5-dichloro-pyridin-3-yl)-benzamide in acetonitrile (10 mL) is heated at 175 C in a microwave reactor for 14 hours. The mixture is cooled to room temperature and concentrated under reduced pressure. The residue is purified by flash silica gel chromatography to give 0.170 g (65.0%) of 3-chloro-N-[5′-chloro-4-(1-hydroxy-ethyl)-3,4,5,6-tetrahydro-2H-[1,2′]bipyridinyl-3′-yl]-benzamide as a yellow oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08952004B2
Source datasetuspto-grants-2015_02
ORD IDord-ea4d7f7ac0354d6581df8ee017e4dead
Source noteuspto-grants-2015_02