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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 344408Generated: October 31, 2026

Acetaldehyde → HCID 53708651, compound

https://huagongshe.com/reaction/344408

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetaldehydeHCID 177—
ReactantMethanolHCID 887—
ReactantSodium HydroxideHCID 14798—
ReactantSodium cyanoborohydrideHCID 5003444—
Reactant4-Amino-N-(1-(5-aminopentyl)piperidin-4-ylmethyl)-5-chloro-2-methoxybenzamideHCID 54008363—
ProductHCID 53708651HCID 53708651—

Reaction Steps

Acetaldehyde (0.32 ml) and sodium cyanoborohydride (0.36 g) were added to a solution of 4-amino-N-(1-(5-aminopentyl)piperidin-4-ylmethyl)-5-chloro-2-methoxybenzamide (1.0 g) in methanol (20 ml), and the mixture was stirred at room temperature for 1 hr. A 10% aqueous sodium hydroxide solution was added to the reaction mixture, and the mixture was extracted with chloroform. The organic layer was washed with saturated brine, dried and the solvent was evaporated under reduced pressure. The obtained residue was purified by silica gel column chromatography (chloroform:methanol=5:1) to give 0.55 g of 4-amino-5-chloro-N-((1-(5-diethylaminopentyl)piperidin-4-yl)methyl)-2-methoxybenzamide.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05864039
Source datasetuspto-grants-1999_01
ORD IDord-95aca08f75d64847ab6ab1525adeb91a
Source noteuspto-grants-1999_01