Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 744926Generated: October 26, 2026

Acetic Acid → N-[2-(3,4-Dichlorophenyl)-4-[4-(2-oxopyrrolidin-1-yl)-piperidino]butyl]-N-methylbenzamide hydrochloride

https://huagongshe.com/reaction/744926

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AcidHCID 176—
ReactantSodium cyanoborohydrideHCID 5003444—
Reactant1-(Piperidin-4-yl)pyrrolidin-2-oneHCID 18314250—
ReactantN-[2-(3,4-Dichlorophenyl)-4-oxobutyl]-N-methylbenzamideHCID 22137499—
SolventMethanolHCID 887—
SolventSodium BicarbonateHCID 516892—
ProductN-[2-(3,4-Dichlorophenyl)-4-[4-(2-oxopyrrolidin-1-yl)-piperidino]butyl]-N-methylbenzamide hydrochlorideHCID 23369936149.4%

Reaction Steps

N-[2-(3,4-Dichlorophenyl)-4-oxobutyl]-N-methylbenzamide (870 mg) in methanol (2.4 mL) was added to a solution of 4-(2-oxopyrrolidin-1-yl)piperidine (0.460 g) and acetic acid (0.16 mL) in methanol (2.4 mL). After 5 minutes, sodium cyanoborohydride (0.173 g) in methanol (2.4 mL) was added in a single portion. After being stirred for 3 hours, the reaction mixture was diluted with aqueous sodium bicarbonate, stirred for 30 minutes, and extracted with dichloromethane. The organic extracts were dried, evaporated, and chromatographed, with dichloromethane:methanol (gradient 98:2, 90:10) as the eluent. The resulting material was dissolved in dichloromethane, precipitated out as the hydrochloride salt with ethereal hydrogen chloride, evaporated, and placed under high vacuum overnight to give the title compound (1.0 g) as a white solid; MS: m/z=502(M+1). Analysis for C27H33Cl2N3O2 ·1.50 HCl: Calculated: C, 58.20; H, 6.24; N, 7.54; Found: C, 58.18; H, 6.27; N, 7.44.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05559132
Source datasetuspto-grants-1996_09
ORD IDord-eaf3ecc101594d8db209cfc8dccb391a
Source noteuspto-grants-1996_09