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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1837760Generated: November 2, 2026

Sodium Bicarbonate → 1-[(5-Chloro-2-methoxy-3-pyridinyl)methyl]-4-[2-(cyclohexylmethyloxy)phenoxymethyl]piperidine

https://huagongshe.com/reaction/1837760

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium BicarbonateHCID 516892—
ReactantSodium triacetoxyborohydrideHCID 5049666—
Reactant5-Chloro-2-methoxynicotinaldehydeHCID 13567757—
Reactant4-[2-(Cyclohexylmethyloxy)phenoxymethyl]piperidineHCID 17837878—
Solvent1,2-DichloroethaneHCID 11—
SolventAcetic AcidHCID 176—
Product1-[(5-Chloro-2-methoxy-3-pyridinyl)methyl]-4-[2-(cyclohexylmethyloxy)phenoxymethyl]piperidineHCID 2267835571%

Reaction Steps

150 mg of 5-chloro-2-methoxy-3-pyridinecarboxaldehyde and 291 mg of 4-[2-(cyclohexylmethyloxy)phenoxymethyl]piperidine were dissolved in 5 ml of 1,2-dichloroethane. To the mixture were added 0.06 ml of acetic acid and 214 mg of sodium triacetoxyborohydride, followed by stirring at room temperature overnight. An aqueous saturated sodium bicarbonate was added to the reaction solution, and then the mixture was extracted with ethyl acetate. The organic layer was washed with water and brine, and then dried over anhydrous magnesium sulfate. The solvent was evaporated, and the crude product was purified by silica gel column chromatography (n-hexane:ethyl acetate=10:1), to give 285 mg of the title compound as a pale yellow oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06784192B2
Source datasetuspto-grants-2004_08
ORD IDord-3d74263829e44d8b98bb18325e81d0f6
Source noteuspto-grants-2004_08