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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1794852Generated: November 3, 2026

4-[(2,4-Dioxo-1,3-thiazolidin-5-yl)methyl]benzene-1-sulfonyl chloride → 4-(2,4-Dioxo-thiazolidin-5-ylmethyl)-N-[4-(4-oxo-piperidin-1-yl)-phenyl]-benzenesulfonamide

https://huagongshe.com/reaction/1794852

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-[(2,4-Dioxo-1,3-thiazolidin-5-yl)methyl]benzene-1-sulfonyl chlorideHCID 15616432—
Reactant1-(4-Amino-phenyl)-piperidin-4-one hydrochlorideHCID 22220240—
Product4-(2,4-Dioxo-thiazolidin-5-ylmethyl)-N-[4-(4-oxo-piperidin-1-yl)-phenyl]-benzenesulfonamideHCID 22220503—

Reaction Steps

The title compound was prepared from 4-(2,4-dioxo-thiazolidin-5-ylmethyl)benzenesulfonylchloride (J. Med. Chem. 1992, 35, 1853) and 1-(4-amino-phenyl)-piperidin-4-one hydrochloride (which was obtained in Example 224) according to the procedure B of Example 225 as a yellowish solid; 1H NMR (300 MHz, DMSO-d6) δ 2.37 (t, J=6.0 Hz, 4 H), 3.10–3.60 (m, 2 H), 3.44 (t, J=6.0 Hz, 4 H), 4.95 (dd, J=12.3, 6.0 Hz, 1 H), 6.80–7.00 (m, 4 H), 7.27 (d, J=8.1 Hz, 2 H), 7.63 (d, J=8.1 Hz, 2 H), 9.77 (brs, 1 H), 12.09 (brs, 1 H); MS (ES) m/z: 459.9 (MH+); HRMS Calcd. for C21H21N3O5S2 M+): 459.0923. Found: 459.0930.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07022716B2
Source datasetuspto-grants-2006_04
ORD IDord-9dfe9ec954e047ca99e2d40df5b919d5
Source noteuspto-grants-2006_04