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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

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantSodium IodideHCID 5238—
Reactant2-Amino-3-(3-chloropropyloxy)pyridineHCID 18936800—
Reactant2,4-Thiazolidinedione sodium saltHCID 86738727—
SolventDimethylformamideHCID 6228—
Product3-[3-(2-Aminopyridin-3-yloxy)propyl]thiazolidine-2,4-dioneHCID 18936799—

Reaction Conditions

Temperature80 °C

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05840732
Source datasetuspto-grants-1998_11
ORD IDord-a122f5d4ee1141fe8b1e32748c526b27
Source noteuspto-grants-1998_11