Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1062467Generated: October 29, 2026

Thiazolidinedione → HCID 131725199, compound

https://huagongshe.com/reaction/1062467

Reaction equation

Participants

RoleNameHCIDCharge
ReactantThiazolidinedioneHCID 5437—
ReactantPiperidinium acetateHCID 3014295—
ReactantHCID 22277850HCID 22277850—
CatalystAcetic AcidHCID 176—
CatalystPiperidineHCID 8082—
SolventTolueneHCID 1140—
ProductHCID 131725199HCID 13172519940.2%

Reaction Steps

To a solution of the title compound of Step B (284 mg, 0.96 mmol) in toluene (16 ml) was added 2,4-thiazolidinedione (140 mg, 1.2 mmol), a catalytic amount of piperidinium acetate which was generated from piperidine (five drops) and acetic acid (five drops) and 4 Å molecular sieves. The mixture was stirred under reflux for about four hours, cooled to room temperature, filtered and concentrated. The product was purified by preparative TLC (4% methanol in dichloromethane) to afford the title compound (153 mg). MS (APCI−) Calc: 395.0, Found: 394.0 (M−1).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06960604B2
Source datasetuspto-grants-2005_11
ORD IDord-6b5aa9c73b1a404b84573df040ec3293
Source noteuspto-grants-2005_11