HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 357145Generated: October 30, 2026
Water → 3-[3-(2-Aminopyridin-3-yloxy)propyl]thiazolidine-2,4-dione
https://huagongshe.com/reaction/357145
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Sodium Iodide | HCID 5238 | — |
| Reactant | 2-Amino-3-(3-chloropropyloxy)pyridine | HCID 18936800 | — |
| Reactant | 2,4-Thiazolidinedione sodium salt | HCID 86738727 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 3-[3-(2-Aminopyridin-3-yloxy)propyl]thiazolidine-2,4-dione | HCID 18936799 | — |
Reaction Steps
To a suspension of 9.33 g (50 mmol) of 2-amino-3-(3-chloropropyloxy)pyridine and 6.97 g (50 mmol) of thiazolidine-2,4-dione sodium salt in 200 ml of N,N-dimethylformamide, 7.49 g (50 mmol) of sodium iodide was added, followed by refluxing 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, n-hexane/ethyl acetate=1/4→ethyl acetate) to yield 8.14 g (60.9%, yellow solid) 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-a122f5d4ee1141fe8b1e32748c526b27 |
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| Source note | uspto-grants-1998_11 |
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