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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1504176Generated: October 30, 2026

3-Pyridinecarboxaldehyde → HCID 67984922, compound

https://huagongshe.com/reaction/1504176

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3-PyridinecarboxaldehydeHCID 10371—
ReactantSodium BicarbonateHCID 516892—
ReactantSodium triacetoxyborohydrideHCID 5049666—
ReactantHCID 70656790HCID 70656790—
Solvent1,2-DichloroethaneHCID 11—
ProductHCID 67984922HCID 67984922—

Reaction Steps

Pyridine-3-carbaldehyde(0.076 ml) was added to a 1,2-dichloroethane solution(3 ml) of 1-methyl-6-{5-[(pyridin-3-ylmethyl)-amino]-pentyloxy}-1H-quinolin-2-one(237 mg). The mixture was stirred for 30 minutes at room temperature. Sodium triacetoxyborohydride(0.23 g) was added to the mixture, and the mixture was stirred at room temperature for 3 days. A saturated sodium hydrogencarbonate aqueous solution was added to the reaction mixture, followed by extraction using dichloromethane. The organic layer was dried with anhydrous sodium sulfate, and condensed under reduced pressure. The residue was purified by NH silica gel column chromatography (ethyl acetate: hexane=1:1). The purified product was condensed under reduced pressure to give the title compound(247 mg) as a yellow oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09212187B2
Source datasetuspto-grants-2015_12
ORD IDord-20361177a0c64077aabd448b53691e45
Source noteuspto-grants-2015_12