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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1726135Generated: November 3, 2026

Sodium hydride → 4-[(4-Bromo-phenyl)-(6-fluoro-pyridin-2-yloxy)-methyl]-piperidine-1-carboxylic acid tert-butyl ester

https://huagongshe.com/reaction/1726135

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium hydrideHCID 24758—
Reactant2,6-DifluoropyridineHCID 73934—
ReactantTert-butyl 4-((4-bromophenyl)(hydroxy)methyl)piperidine-1-carboxylateHCID 57603260—
SolventDimethylformamideHCID 6228—
Product4-[(4-Bromo-phenyl)-(6-fluoro-pyridin-2-yloxy)-methyl]-piperidine-1-carboxylic acid tert-butyl esterHCID 6897287294%

Reaction Steps

To a solution of 4-[(4-bromo-phenyl)-hydroxy-methyl]-piperidine-1-carboxylic acid tert-butyl ester (1.36 g, 3.67 mmol) in DMF (18 mL) was added NaH (60% in mineral oil, 367 mg, 9.17 mmol) and the mixture was stirred at room temperature for 10 minutes. 2,6-Difluoropyridine (1.00 mL, 11.0 mmol) was added and the mixture was heated at 70° C. overnight. Work-up and purification gave 4-[(4-bromo-phenyl)-(6-fluoro-pyridin-2-yloxy)-methyl]-piperidine-1-carboxylic acid tert-butyl ester as an off-white solid (1.60 g, 94%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07491735B2
Source datasetuspto-grants-2009_02
ORD IDord-92f496bb81ca4d4aa16190d1aa66630a
Source noteuspto-grants-2009_02