HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 248126Generated: October 26, 2026
2H-thiopyran-2-one → 10-amino-3,4-dihydro-7-fluoro-1H-thiopyrano [4,3-b]quinoline
https://huagongshe.com/reaction/248126
Participants
| Role | Name | HCID | Charge |
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| Reactant | 2H-thiopyran-2-one | HCID 638002 | — |
| Reactant | 2-Amino-4-fluorobenzonitrile | HCID 9942158 | — |
| Catalyst | Zincchloride | HCID 3007855 | — |
| Solvent | Nitrobenzene | HCID 7416 | — |
| Product | 10-amino-3,4-dihydro-7-fluoro-1H-thiopyrano [4,3-b]quinoline | HCID 14580247 | 62.4% |
Reaction Steps
A mixture of 4-fluoroanthranilonitrile (4.47 g) and freshly fused, pulverized ZnCl2 (6.7 g) in 20 ml of nitrobenzene was heated at 50° C. for 45 minutes. To the resulting suspension was added thiopyran-2-one (5.1 g). This was heated at 130° C. for 3 hours. The resulting precipitate was filtered, rinsed with ether and partioned between 2-butanone and NH4OH solution. The aqueous layer was extracted with 2-butanone and the combined organics were washed with water and dried (MgSO4). This resulted in 4.8 g of a tan solid, m.p. 234°-237° C. d., which was recrystallized from ethyl acetate to give 3.0 g of a white powder, m.p. 235°-237° C. d.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05208330 |
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| Source dataset | uspto-grants-1993_05 |
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| ORD ID | ord-708aac1893fd453c8b8245ce18efd0c6 |
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| Source note | uspto-grants-1993_05 |
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