HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 864021Generated: October 24, 2026
Water → 1,3-bis[4-(2-pyridylthio)butyl]quinazoline-2,4(1H,3H)-dione
https://huagongshe.com/en/reaction/864021
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Quinazolinedione | HCID 64048 | — |
| Reactant | 1,8-Diazabicyclo(5.4.0)undec-7-ene | HCID 81184 | — |
| Reactant | 2-(4-Chlorobutylthio)pyridine | HCID 19079186 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 1,3-bis[4-(2-pyridylthio)butyl]quinazoline-2,4(1H,3H)-dione | HCID 19079232 | 9% |
Reaction Steps
To a solution of 1.62 g (10 mmol) of benzoylene urea and 2.02 g (10 mmol) of 2-(4-chlorobutylthio)pyridine in 50 ml of dimethylformamide, 1.65 ml (11mmol) of 1,8-diazabicyclo[5.4.0]-7-undecene was added, and the mixture was stirred at 80° C. for 16 hours. After cooling, water was added to the reaction mixture, and the mixture was extracted with ethyl acetate. The extract was dried and the solvent was distilled off. The residue was purified by column chromatography (eluent:hexane/ethyl acetate=2:1 to 1:2). First, 221 mg of the desired product was obtained (4.6% yield, yellow oil), and then, 292 mg of 3-[4-(2-pyridylthio)butyl]quinazoline-2,4(1H,3H)-dione was obtained (8.9% yield, white crystals).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05561147 |
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| Source dataset | uspto-grants-1996_10 |
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| ORD ID | ord-9d3f66780e5642d3a4d5c2da31efc980 |
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| Source note | uspto-grants-1996_10 |
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