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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 969664Generated: October 30, 2026

4-Pyridinecarboxaldehyde → HCID 10343318, compound

https://huagongshe.com/reaction/969664

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-PyridinecarboxaldehydeHCID 13389—
ReactantSodium borohydrideHCID 4311764—
ReactantHCID 69510665HCID 69510665—
SolventEthanolHCID 702—
ProductHCID 10343318HCID 10343318—

Reaction Steps

A mixture of 2-amino-N-{4-[1-methyl-1-(1-methyl-piperidin-4-yl)ethyl]phenyl}benzamide (600 mg, Step B) and 4-pyridinecarboxaldehyde (0.22 mL) was heated at reflux in EtOH (50 mL) overnight. NaBH4 (250 mg) was added and the mixture was heated at reflux for 10 min and evaporated. The residue was mixed with CH2Cl2 and washed with H2O twice, followed by brine. The organic layer was dried over Na2SO4 and evaporated under reduced pressure. The residue was purified by column chromatography using 10% MeOH/CH2Cl2 to provide the title compound. MS (ES+): 443 (M+H)+. Calc'd. for C28H34N4O-442.27.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07307088B2
Source datasetuspto-grants-2007_12
ORD IDord-1c1a2b8012e747229cfa1d19629dbef4
Source noteuspto-grants-2007_12