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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1369142Generated: October 30, 2026

Piperidin-4-ol → HCID 10302804, compound

https://huagongshe.com/reaction/1369142

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPiperidin-4-olHCID 79341—
ReactantDiisopropylethylamineHCID 81531—
ReactantN-(3,5-bis-trifluoromethyl-benzyl)-6-chloro-N-methyl-4-o-tolyl-nicotinamideHCID 10277890—
Catalyst4-(Dimethylamino)pyridineHCID 14284—
SolventWaterHCID 962—
SolventDichloromethaneHCID 6344—
ProductHCID 10302804HCID 1030280480%

Reaction Conditions

Temperature140 °C

Reaction Steps

A mixture of 10.0 g (20.5 mmol) N-(3,5-bis-trifluoromethyl-benzyl)-6-chloro-N-methyl-4-o-tolyl-nicotinamide, 3.1 g (31 mmol) 4-hydroxypiperidine, 10.6 ml (62 mmol) N-ethyldiisopropylamine and 0.13 g (1.0 mmol) 4-(N,N-dimethylamino)-pyridine was stirred at 140° C. for 70 h. After cooling to room temperature the residue was dissolved in a mixture of dichloromethane and water. The layers were separated and the aqueous layer was extracted with four portions of dichloromethane. The combined organic extracts were dried with sodium sulfate and concentrated to give 11.1 g of crude product. Flash chromatography afforded 9.0 g (80%) of the title compound as a white solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06576762B2
Source datasetuspto-grants-2003_06
ORD IDord-120528db7e994abbbf1eea97b590c70a
Source noteuspto-grants-2003_06