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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 343465Generated: October 26, 2026

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

https://huagongshe.com/reaction/343465

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AcidHCID 176—
ReactantSodium cyanoborohydrideHCID 5003444—
Reactant3-(Piperidin-4-yl)-1,3-oxazolidin-2-oneHCID 13060627—
ReactantN-[2-(3,4-Dichlorophenyl)-4-oxobutyl]-N-methylbenzamideHCID 22137499—
SolventMethanolHCID 887—
SolventSodium BicarbonateHCID 516892—
ProductN-[2-(3,4-Dichlorophenyl)-4-[4-(2-oxo-1,3-oxazolidin-3-yl)piperidino]butyl]-N-methylbenzamide hydrochlorideHCID 22137563138.5%

Reaction Steps

N-[2-(3,4-Dichlorophenyl)-4-oxobutyl]-N-methylbenzamide (0.823 g) in methanol (4 mL) was added to a solution of 4-(2-oxo-1,3-oxazolidin-3-yl)piperidine (0.600 g) and acetic acid (0.20 mL) in methanol (8 mL). After 5 minutes, sodium cyanoborohydride (0.220 g) in methanol (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 eluent. The resulting material was dissolved in dichloromethane, precipitated as the hydrochloride salt with ethereal hydrogen chloride, evaporated, and placed under high vacuum overnight to give the title compound as a white solid (0.88 g); MS: m/z=504(M+l); Analysis for C26H31Cl2N3O3.1.20 HCl: Calculated: C, 56.96; H, 5.92; N, 7.66; Found: C, 57.02; H, 6.05; N, 7.62.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05861392
Source datasetuspto-grants-1999_01
ORD IDord-529ad33c286f4acb9dd811e9c9e2868c
Source noteuspto-grants-1999_01