Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Thiourea | HCID 2723790 | — |
| Reactant | 4-Chloro-7-nitroquinoline | HCID 12322580 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | 7-Nitroquinoline-4(1H)-thione | HCID 19075066 | — |
Reaction Steps
4-Chloro-7-nitroquinoline (100 mg, 0.48 mmol) and thiourea (100 mg, 1.3 mmol) were added to ethanol (50 ml) and stirred at 80° C. for 30 minutes. After allowing to cool to room temperature, ethanol was removed under reduced pressure. The residue was chromatographed by silica gel column chromatography and eluted with mixed solution of methylene chloride with methanol (19 : 1) for collection of yellow bands. The solvent was removed to obtain 7 mg (7%) of the titled yellow compound.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05773449 |
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| Source dataset | uspto-grants-1998_06 |
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| ORD ID | ord-a6262e162148456bb565a1479526dd3f |
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| Source note | uspto-grants-1998_06 |
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