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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2093587Generated: October 31, 2026

Potassium Carbonate → HCID 131730589, compound

https://huagongshe.com/reaction/2093587

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium CarbonateHCID 11430—
ReactantTert-butyl (piperidin-4-ylmethyl)carbamateHCID 723429—
Reactant2-Bromo-5-(trifluoromethyl)pyridineHCID 2736434—
SolventMethanolHCID 887—
ProductHCID 131730589HCID 13173058981%

Reaction Conditions

Temperature120 °C

Reaction Steps

In a 5-ml microwave vial equipped was placed potassium carbonate (1.38 g), tert-butyl(piperidin-4-ylmethyl)carbamate (1.07 g), and 2-bromo-5-trifluoromethylpyridine (1.13 g) in methanol. This was heated to 120° C. for 30 min in a microwave reactor. The mixture was cooled and concentrated in vacuo, and the residue was taken up in ethyl acetate. This was filtered through a plug of silica gel, and the eluent was concentrated in vacuo to provide tert-butyl({1-[5-(trifluoromethyl)pyridin-2-yl]piperidin-4-yl}methyl)carbamate (1.45 g, 81%). This compound was taken up in 15 ml of dichloromethane and 15 ml of trifluoroacetic acid. The resultant mixture was stirred at room temperature for 2 h, and then concentrated and taken up in dichloromethane (20 ml) and saturated aqueous sodium bicarbonate. The mixture was extracted and the organic layer was dried over sodium sulfate, filtered, and concentrated in vacuo to provide 1.31 g (87%) of the title compound. Mass spectrum (ESI) 260.1 (M+1).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08445480B2
Source datasetuspto-grants-2013_05
ORD IDord-442c14bc918343bf9334b186870f21db
Source noteuspto-grants-2013_05