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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 343471Generated: October 26, 2026

N-[2-(3,4-Dichlorophenyl)-4-oxobutyl]-N-methylbenzamide → (S)-N-[2-(3,4-Dichlorophenyl)-4-[4-(3-methyl-2-thioxoperhydropyrimidin-1-yl)piperidino]butyl]-N-methylbenzamide hydrochloride

https://huagongshe.com/reaction/343471

Reaction equation

Participants

RoleNameHCIDCharge
ReactantN-[2-(3,4-Dichlorophenyl)-4-oxobutyl]-N-methylbenzamideHCID 22137499—
Reactant4-(3-Methyl-2-thioxoperhydropyrimidin-1-yl)piperidineHCID 22137509—
Product(S)-N-[2-(3,4-Dichlorophenyl)-4-[4-(3-methyl-2-thioxoperhydropyrimidin-1-yl)piperidino]butyl]-N-methylbenzamide hydrochlorideHCID 86589869—

Reaction Steps

Using the procedure of Example 1, replacing 4-(2-oxo-1,3-oxazolidin-3-yl)piperidine with 4-(3-methyl-2-thioxoperhydropyrimidin-1-yl)-piperidine, and N-[2-(3,4-dichlorophenyl)-4-oxobutyl]-N-methylbenzamide with the (S)-enantiomer, the title compound was obtained as a white solid; MS: m/z=547(M+1); Analysis for C28H36Cl2N4OS.1.70 HCl.0.10 (C2H5)2O: Calculated: C, 55.28; H, 6.32; N, 9.08; Found: C, 55.21; H, 6.37; N, 8.88.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05861392
Source datasetuspto-grants-1999_01
ORD IDord-c71586b5f0de49c0ad3e1da9aa735b4d
Source noteuspto-grants-1999_01