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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1370204Generated: October 30, 2026

Piperidine → 5-[4-(2,2-Diethoxy-ethoxy)-benzylidene]-2-piperidin-1-yl-thiazol-4-one

https://huagongshe.com/reaction/1370204

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPiperidineHCID 8082—
ReactantRhodanineHCID 1201546—
Reactant5-[4-(2,2-Diethoxy-ethoxy)-benzylidene]-2-thioxo-thiazolidin-4-oneHCID 73990608—
SolventEthanolHCID 702—
Product5-[4-(2,2-Diethoxy-ethoxy)-benzylidene]-2-piperidin-1-yl-thiazol-4-oneHCID 6992288669.2%

Reaction Steps

A mixture of 5-[4-(2,2-diethoxy-ethoxy)-benzylidene]-2-thioxo-thiazolidin-4-one (which was obtained in Intermediate 37)(1.19 g, 5 mmol), rhodanine (0.67 g, 5 mmol) and piperidine (1.72 g, 20.2 mmol) in ethanol (50 mL) was refluxed for 2 hours. After cooling to room temperature hexanes (70 mL) were added and the solid which was formed was collected to give the title compound as a yellowish solid (1.4 g, 69%); 1H NMR (300 MHz, DMSO-d6) δ 1.14(t, J =7.1 Hz, 6 H), 1.55-1.75(m, 6 H), 3.40-3.80 (m, 6 H), 3.85-3.95(m, 2 H), 4.02(d, J=5.2 Hz, 2 H), 4.82 (t, J=5.2 Hz, 1 H), 7.11 (d, J=7.6 Hz, 2 H), 7.57 (d, J=7.6 Hz, 2 H), 7.58(s, 1 H); MS (ES) m/z: 404.9 (MH+, 100%); HRMS Calcd. for C21H28N2O4S (M+): 404.1770. Found: 404.1780.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06583140B2
Source datasetuspto-grants-2003_06
ORD IDord-0ae7766abfe24a8996a7fe48217efbfe
Source noteuspto-grants-2003_06