HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 357003Generated: October 30, 2026
Water → 3-[5-(Imidazo[1,2-a]pyridin-5-yl)pentyl]thiazolidine-2,4-dione
https://huagongshe.com/reaction/357003
Participants
| Role | Name | HCID | Charge |
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| Reactant | Water | HCID 962 | — |
| Reactant | 5-(5-Chloropentylthio)imidazo[1,2-a]pyridine | HCID 18936743 | — |
| Reactant | 2,4-Thiazolidinedione sodium salt | HCID 86738727 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 3-[5-(Imidazo[1,2-a]pyridin-5-yl)pentyl]thiazolidine-2,4-dione | HCID 18936821 | — |
Reaction Steps
A suspension of 2.22 g (10 mmol) of 5-(5-chloropentylthio)imidazo[1,2-a]pyridine and 1.40 g (10 mmol) of thiazolidine-2,4-dione sodium salt in 30 ml of N,N-dimethylformamide was heated at 80° C. for 16 hours. After cooling, the reaction mixture was poured into water, extracted with ethyl acetate, washed with water and dried, after which the solvent was distilled off. The residue was purified by column chromatography (eluent: ethyl acetate→ethyl acetate/ethanol=10/1) to yield 1.56 g (51.4%, light brown oily substance) of the desired product.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05840732 |
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| Source dataset | uspto-grants-1998_11 |
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| ORD ID | ord-1e98cee1341a44dd8329c2949aa00392 |
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| Source note | uspto-grants-1998_11 |
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