HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 357013Generated: October 30, 2026
Sodium Iodide → 3-[2-(Imidazo[1,2-a]pyridin-5-yl)ethyl]thiazolidine-2,4-dione
https://huagongshe.com/reaction/357013
Participants
| Role | Name | HCID | Charge |
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| Reactant | Sodium Iodide | HCID 5238 | — |
| Reactant | Thionyl Chloride | HCID 24386 | — |
| Reactant | 2-(Imidazo[1,2-a]pyridin-5-yl)ethanol | HCID 21265869 | — |
| Reactant | 2,4-Thiazolidinedione sodium salt | HCID 86738727 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Chloroform | HCID 6212 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 3-[2-(Imidazo[1,2-a]pyridin-5-yl)ethyl]thiazolidine-2,4-dione | HCID 18936757 | — |
Reaction Steps
To a suspension of 4.0 g (24.7 mmol) of 5-(2-hydroxyethyl)imidazo[1,2-a]pyridine in 30 ml of chloroform, 5 ml (68 mmol) of thionyl chloride was added. After refluxing for 2 hours, the solvent was distilled off. To a suspension of the residue and 8.36 g (60 mmol) of 2,4-thiazolidinedione sodium salt in 50 ml of N,N-dimethylformamide, 3.75 g (25 mmol) of sodium iodide was added, followed by stirring at 80° C. for 16 hours. After the reaction mixture was cooled, water was added. The reaction mixture was then extracted with ethyl acetate and dried, after which the solvent was distilled off. The residue was purified by column chromatography (eluent: n-hexane/ethyl acetate=2/1→1/1→1/4) to yield 1.00 g (15.5%, light orange powder) 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-8022d0eff17842dc9617562550dc138d |
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| Source note | uspto-grants-1998_11 |
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