Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2221080Generated: October 30, 2026

Acetic Acid → HCID 10207981, compound

https://huagongshe.com/reaction/2221080

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AcidHCID 176—
ReactantSodium cyanoborohydrideHCID 5003444—
Reactant(S)-N-[2-(3,4-Dichlorophenyl)-4-oxobutyl]-N-methylbenzamideHCID 15381108—
Reactant[1,4'-Bipiperidin]-2-oneHCID 21839852—
SolventMethanolHCID 887—
SolventSodium BicarbonateHCID 516892—
ProductHCID 10207981HCID 1020798198.6%

Reaction Steps

(S)—N-[2-(3,4-Dichlorophenyl)-4-oxobutyl]-N-methylbenzamide (0.78 g) in methanol (3 mL) was added to a solution of [1,4′]bipiperidinyl-2-one (0.34 g) and acetic acid (0.15 mL) in methanol (8 mL). After 10 minutes, sodium cyanoborohydride (0.17 g) in methanol (4 mL) was added in a single portion. After being stirred overnight, the reaction mixture was diluted with saturated aqueous sodium bicarbonate, stirred for 30 minutes, and extracted with dichloromethane (4×50 mL). The organic extracts were dried, evaporated, and purified by chromatography, with dichloromethane:methanol (gradient 95:5, 90:10) as eluent to give the title compound (0.95 g). MS: m/z=516(M+). The product was dissolved in methanol (2 mL) and citric acid was added. The solution was concentrated and the residue was triturated with ether. The product was obtained as a white foam (1.2 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07368461B2
Source datasetuspto-grants-2008_05
ORD IDord-876dc7352ca84eb78283d770c4fc311d
Source noteuspto-grants-2008_05