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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 744928Generated: October 30, 2026

(S)-N-[2-(3,4-Dichlorophenyl)-4-oxobutyl]-N-methylbenzamide → (S)-N-[2-(3,4-Dichlorophenyl)-4-[4-(2-oxo-1,2,5,6-tetrahydropyrid-1-yl)piperidino]butyl]-N-methylbenzamide hydrochloride

https://huagongshe.com/reaction/744928

Reaction equation

Participants

RoleNameHCIDCharge
Reactant(S)-N-[2-(3,4-Dichlorophenyl)-4-oxobutyl]-N-methylbenzamideHCID 15381108—
ReactantN-[2-(3,4-Dichlorophenyl)-4-oxobutyl]-N-methylbenzamideHCID 22137499—
Reactant4-(2-Oxo-1,2,5,6-tetrahydropyrid-1-yl)piperidineHCID 23369958—
Product(S)-N-[2-(3,4-Dichlorophenyl)-4-[4-(2-oxo-1,2,5,6-tetrahydropyrid-1-yl)piperidino]butyl]-N-methylbenzamide hydrochlorideHCID 67747255—

Reaction Steps

Using a procedure similar to that described in Example 7, except replacing 4-(2-oxopyrrolidin-1-yl)piperidine with 4-(2-oxo-1,2,5,6-tetrahydropyrid-1-yl)piperidine and N-[2-(3,4-dichlorophenyl)-4-oxobutyl]-N-methylbenzamide with (S)-N-[2-(3,4-dichlorophenyl)-4-oxobutyl]-N-methylbenzamide, the title compound was obtained as a white solid; MS: m/z=514(M+1). Analysis for C28H33Cl2N3O2 ·2.50 HCl·0.30 Et2O: Calculated: C, 55.86; H, 6.18; N, 6.69; Found: C, 55.83; H, 6.43; N, 6.66.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05559132
Source datasetuspto-grants-1996_09
ORD IDord-7584d033bceb4e2b8985a2ef6d6eabd7
Source noteuspto-grants-1996_09