HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 357062Generated: October 25, 2026
Water → 3-[4-(Imidazo[1,2-a]pyridin-5-ylthio)-butyl]hydantoin
https://huagongshe.com/reaction/357062
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Hydantoin | HCID 10006 | — |
| Reactant | 1,8-Diazabicyclo(5.4.0)undec-7-ene | HCID 81184 | — |
| Reactant | Imidazo[1,2-a]pyridine,5-[(4-chlorobutyl)thio]- | HCID 18936641 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 3-[4-(Imidazo[1,2-a]pyridin-5-ylthio)-butyl]hydantoin | HCID 18936665 | — |
Reaction Steps
To a solution of 2.41 g (10.0 mmol) of 5-(4-chlorobutylthio)imidazo[1,2-a]pyridine and 1.00 g (10.0 mmol) of hydantoin in 30 ml of N,N-dimethylformamide, 1.50 ml (10.0 mmol) of 1,8-diazabicyclo[5.4.0]-7-undecene was added, followed by stirring at 80° C. for 16 hours. After the reaction mixture was cooled, water was added; the mixture was extracted with ethyl acetate and dried, after which the solvent was distilled off. The residue was purified by column chromatography (eluent, chloroform/methanol=20/1→10/1) to yield 1.27 g (41.7%, 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-356bb265275d412ca0d7a303c808ed76 |
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| Source note | uspto-grants-1998_11 |
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