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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 725111Generated: October 26, 2026

4-(2-(Methylsulfinyl)phenyl)piperidine → 3-[1-(3,4-Dichlorophenyl)-3-[4-(2-methylsulfinylphenyl)-piperidino)propyl]-2-ethyl-2,3-dihydroisoindol-1-one hydrochloride

https://huagongshe.com/reaction/725111

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-(2-(Methylsulfinyl)phenyl)piperidineHCID 18700387—
Reactant3-(3,4-dichlorophenyl)-3-(2-ethyl-3-oxo-2,3-dihydro-1H-isoindol-1-yl)propionaldehydeHCID 21839751—
Product3-[1-(3,4-Dichlorophenyl)-3-[4-(2-methylsulfinylphenyl)-piperidino)propyl]-2-ethyl-2,3-dihydroisoindol-1-one hydrochlorideHCID 2183991498.6%

Reaction Steps

3-(3,4-Dichlorophenyl)-3-(2-ethyl-3-oxo-2,3-dihydro-1H-isoindol-1-yl)propionaldehyde (0.24 g) and 4-(2-methylsulfinylphenyl)piperidine (0.224 g) were coupled using conditions similar to those described Example 1 to give the title compound (0.198 g); mp 150° C. (dec); MS: m/z=571(M+1); NMR (CD3OD): 1.3 (m,3), 2.0 (m,6), 2.6 (m,1), 3.3 (m,12), 5.05 (m,1), 7.28 (m,11). Analysis for C31H34Cl2N2O2S.1.0 HCl.0.9 H2O: Calculated: C, 59.83; H, 5.96; N, 74.50; Found: C, 59.55; H, 5.76; N, 4.89.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05705505
Source datasetuspto-grants-1998_01
ORD IDord-a7c6adfc52de4e6685cbba81c0fd7272
Source noteuspto-grants-1998_01