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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2269306Generated: October 30, 2026

Thiazolidinedione → HCID 88215764, compound

https://huagongshe.com/reaction/2269306

Reaction equation

Participants

RoleNameHCIDCharge
ReactantThiazolidinedioneHCID 5437—
ReactantPiperidineHCID 8082—
ReactantHCID 131723013HCID 131723013—
SolventEthanolHCID 702—
ProductHCID 88215764HCID 8821576487%

Reaction Steps

The title compound of Example 16 (580 mg, 1.7 mmol), piperidine (30 mg, 0.34 mmol) and 2,4thiazolidinedione (405 mg, 3.4 mmol) were combined in ethanol (20 mL) and the resulting solution was refluxed overnight. The solvent was removed in vacuo and the residue was purified on silica gel, eluting with hexane/ethyl acetate (3/1) plus 5% acetic acid, to afford the title compound as a solid (640 mg, 87%). mp 205-206° C. 1HNMR (300 MHz, DMSO-d6): δ2.0 (m, 2H), 2.3 (s, 3H), 2.4 (t, 2H), 3.1 (s, 3H), 4.2 (dd, 1H), 7.4 (m, 5H), 7.6 (d, 2H), 7.7 (s, 1H), 7.9 (m, 2H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06329408B1
Source datasetuspto-grants-2001_12
ORD IDord-062d933aebc141b686292e4e2ff5b687
Source noteuspto-grants-2001_12