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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 25039Generated: October 26, 2026

Water → 4-[4-(t-Butoxycarbonylamino)methyl-4-hydroxypiperidin-1-yl]pyridine 1-Oxide

https://huagongshe.com/reaction/25039

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
Reactant4-chloropyridine N-oxideHCID 70724—
ReactantSodium BicarbonateHCID 516892—
Reactanttert-butyl N-((4-hydroxypiperidin-4-yl)methyl)carbamateHCID 10868112—
SolventIsoamyl AlcoholHCID 31260—
Product4-[4-(t-Butoxycarbonylamino)methyl-4-hydroxypiperidin-1-yl]pyridine 1-OxideHCID 1103465836.8%

Reaction Steps

To a suspension in isoamyl alcohol (35 ml) of conventionally known compounds: 4-[(t-butoxycarbonylamino)methyl]-4-hydroxypiperidine (2.00 g) and 4-chloropyridine 1-oxide (1.12 g), was added sodium hydrogencarbonate (1.75 g) and the mixture was heated under reflux for 4 hours. The reaction mixture was allowed to cool and water was added thereto. The reaction mixture was extracted with methylene chloride and the organic layer was washed with saturated sodium chloride solution and dried over anhydrous sodium sulfate. The solvent was distilled off under reduced pressure and the resulting residue was purified by silica gel column chromatography (eluent:methylene chloride:methanol=9:1-4:1) to obtain the title compound (1.03 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06858599B2
Source datasetuspto-grants-2005_02
ORD IDord-784990b1458d4facbd2c0e6fab5babbd
Source noteuspto-grants-2005_02