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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 74901Generated: October 23, 2026

Pyridine → Tert-butyl 2-carbamoyl-4,4-difluoropiperidine-1-carboxylate

https://huagongshe.com/en/reaction/74901

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPyridineHCID 1049—
ReactantAmmonium BicarbonateHCID 14013—
ReactantDi-tert-butyl dicarbonateHCID 90495—
Reactant1-((Tert-butoxy)carbonyl)-4,4-difluoropiperidine-2-carboxylic acidHCID 10106900—
Solvent1,4-DioxaneHCID 31275—
ProductTert-butyl 2-carbamoyl-4,4-difluoropiperidine-1-carboxylateHCID 67286514—

Reaction Steps

To a solution of 1-tert-butoxycarbonyl-4,4-difluoro-piperidine-2-carboxylic acid, 13f, (1.67 g, 6.30 mmol) in 1,4-dioxane (12 mL) was added pyridine (0.35 mL, 4.33 mmol), followed by di-tert-butyl dicarbonate (1.78 g, 8.17 mmol) and ammonium bicarbonate (0.63 g, 7.86 mmol). The reaction mixture was stirred at room temperature overnight. The solvent was removed under reduced pressure and the residue was taken up in EtOAc. The organic phase was washed with water, aqueous saturated KHSO4 solution, brine, dried over Na2SO4, filtered and evaporated to dryness. The crude residue was used without further purification.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08829007B2
Source datasetuspto-grants-2014_09
ORD IDord-e7fe087c2d5d46bab2cfd714b40831b4
Source noteuspto-grants-2014_09