HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 357141Generated: October 26, 2026
Water → 3-[4-(Imidazo[1,2-a]pyridin-5-ylsulfonyl)butyl]thiazolidine-2,4-dione
https://huagongshe.com/reaction/357141
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Thiazolidinedione | HCID 5437 | — |
| Reactant | 1,8-Diazabicyclo[5.4.0]undec-2-ene | HCID 9812821 | — |
| Reactant | 5-(4-Chlorobutylsulfonyl)imidazo[1,2-a]pyridine | HCID 18936865 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 3-[4-(Imidazo[1,2-a]pyridin-5-ylsulfonyl)butyl]thiazolidine-2,4-dione | HCID 18936763 | — |
Reaction Steps
To a solution of 0.27 g (1.0 mmol) of 5-(4-chlorobutylsulfonyl)imidazo[1,2-a]pyridine and 0.177 g (1.0 mmol) of thiazolidine-2,4-dione in 7 ml of N,N-dimethylformamide, 0.15 ml (1.0 mmol) of 1,8-diazabicyclo[5.4.0]-undecene was added, followed by heating 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, chloroform→chloroform/methanol=50/1) to yield 0.22 g (62.2%, light yellow 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-6bf2f688afb946ceb7d2131c8f22c8fa |
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| Source note | uspto-grants-1998_11 |
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