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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2068696Generated: November 1, 2026

Water → tert-Butyl 3-[(4-bromo-2-oxopyridin-1(2H)-yl)methyl]piperidine-1-carboxylate

https://huagongshe.com/reaction/2068696

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantPotassium HydroxideHCID 14797—
Reactant1-Boc-3-bromomethylpiperidineHCID 21188531—
ReactantHCID 178515446HCID 178515446—
SolventDimethyl SulfoxideHCID 679—
Producttert-Butyl 3-[(4-bromo-2-oxopyridin-1(2H)-yl)methyl]piperidine-1-carboxylateHCID 6873384595%

Reaction Steps

To a solution of 2-hydroxy-4-bromopyridine (0.10 g, 0.57 mmol) in DMSO (1.50 mL) was added KOH (0.095 g, 1.70 mmol) and the resulting reaction mixture was stirred for 10 min at room temperature followed by addition of 1-Boc-3-bromomethylpiperidine (0.16 g, 0.57 mmol). The reaction mixture was then stirred at 45° C. for 16 h. After the completion of reaction (TLC monitoring), water was added to the reaction and extracted with EtOAc (3×25 mL). The combined organics was washed with brine, dried (Na2SO4), filtered and concentrated. The residue was purified over silica gel (100-200 M, 1% MeOH-DCM) to obtain the desired product (0.15 g, 95%). MS: 371.10 (M+H)+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08299065B2
Source datasetuspto-grants-2012_10
ORD IDord-8aae24412ae143088d3032618860ce99
Source noteuspto-grants-2012_10