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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1187377Generated: November 1, 2026

Hydrochloric Acid → methyl {(3S)-1-[5-(adamantan-1-ylcarbamoyl)-6-(propylthio)pyridin-2-yl]piperidin-3-yl}acetate

https://huagongshe.com/reaction/1187377

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantPotassium CarbonateHCID 11430—
Reactantmethyl 2-[(3S)-piperidin-3-yl]acetateHCID 40153895—
ReactantN-adamantan-1-yl-6-chloro-2-(propylthio)nicotinamideHCID 59830706—
SolventButyronitrileHCID 8008—
SolventEthyl AcetateHCID 8857—
Productmethyl {(3S)-1-[5-(adamantan-1-ylcarbamoyl)-6-(propylthio)pyridin-2-yl]piperidin-3-yl}acetateHCID 5983077044%

Reaction Steps

N-adamantan-1-yl-6-chloro-2-(propylthio)nicotinamide (0.365 g, 1 mmol) was added to (S)-methyl 2-(piperidin-3-yl)acetate.HCl (0.194 g, 1 mmol) and potassium carbonate (0.415 g, 3 mmol) in butyronitrile (4 mL) was heated at 150° C. for 2 hours. The reaction mixture was diluted with EtOAc (50 mL), and washed sequentially with water (20 mL) and brine (20 mL). The organic layer was dried over MgSO4, filtered and evaporated to afford crude product. The crude product was purified by flash silica chromatography, elution gradient 0 to 50% EtOAc in hexane. Pure fractions were evaporated to dryness to afford methyl {(3S)-1-[5-(adamantan-1-ylcarbamoyl)-6-(propylthio)pyridin-2-yl]piperidin-3-yl}acetate (0.215 g, 44%) as a white solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08673938B2
Source datasetuspto-grants-2014_03
ORD IDord-7174c585e1974e7684df259981f3383f
Source noteuspto-grants-2014_03