HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 6184Generated: October 26, 2026
Water → 1,3-bis[4-(4-pyridylthio)butyl]quinazoline-2(1H)-thion-4(3H)-one
https://huagongshe.com/reaction/6184
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Water | HCID 962 | — |
| Reactant | 1,8-Diazabicyclo(5.4.0)undec-7-ene | HCID 81184 | — |
| Reactant | 4-(4-Chlorobutylthio)pyridine | HCID 15816978 | — |
| Reactant | 3-[4-(4-pyridylthio)butyl]quinazoline-2(1H)-thion-4(3H)-one | HCID 131718180 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 1,3-bis[4-(4-pyridylthio)butyl]quinazoline-2(1H)-thion-4(3H)-one | HCID 131718179 | 97.1% |
Reaction Steps
To a solution of 515 mg (1.5 mmol) of 3-[4-(4-pyridylthio)butyl]quinazoline-2 (1H)-thion-4(3H)-one and 332 mg (1.65 mmol) of 4-(4-chlorobutylthio)pyridine in 15 ml of dimethylformamide, 0.25 ml (1.65 mmol) 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 flash column chromatography (eluent: ethyl acetate/ethanol =25:1 to 10:1) to give 0.694 mg of the desired product (97.1% yield; colorless oil).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05246948 |
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| Source dataset | uspto-grants-1993_09 |
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| ORD ID | ord-190cc34a0d224df4a3612d1206af180e |
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| Source note | uspto-grants-1993_09 |
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