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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1249723Generated: November 4, 2026

4-(4-Piperidyl)pyridine → 1-Tert-butoxycarbonyl-4-[4-(4-pyridyl)-1-piperidylmethyl]piperidine

https://huagongshe.com/reaction/1249723

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-(4-Piperidyl)pyridineHCID 1139597—
Reactanttert-Butyl 4-formylpiperidine-1-carboxylateHCID 1514430—
ReactantSodium cyanoborohydrideHCID 5003444—
SolventAcetic acid methanolHCID 10129899—
Product1-Tert-butoxycarbonyl-4-[4-(4-pyridyl)-1-piperidylmethyl]piperidineHCID 1832891437.8%

Reaction Steps

To a solution of 1-(tert-butoxycarbonyl)-4-(formyl)piperidine (2.59 g) and 4-(4-pyridyl)piperidine (1.97 g) in methanol/acetic acid (99:1) was added sodium cyanoborohydride (2.29 g) portionwise over 30 minutes and the resultant suspension stirred at ambient temperature for 3 hours. The suspension was quenched by addition of saturated aqueous sodium bicarbonate solution and the resulting mixture extracted with ethyl acetate. The organic phase was dried (Na2SO4) and evaporated. The residue was purified by chromatography eluting with 5% methanol in dichloromethane to give 1-tert-butoxycarbonyl-4-[4-(4-pyridyl)-1-piperidylmethyl]piperidine (1.65 g) as a solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06335341B1
Source datasetuspto-grants-2002_01
ORD IDord-3eec01a6f9034ddb93efd3f1c4cc94b7
Source noteuspto-grants-2002_01