HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 521413Generated: October 29, 2026
1,4-Dioxane → Methyl 3-fluoro-11-oxo-6,7,8,9,10,11-hexahydro-5H-cyclohepta[b]quinoline-1-carboxylate
https://huagongshe.com/reaction/521413
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 1,4-Dioxane | HCID 31275 | — |
| Reactant | Methyl 2-oxocycloheptane-1-carboxylate | HCID 288225 | — |
| Reactant | Methyl 3-amino-5-fluorobenzoate | HCID 3807862 | — |
| Solvent | Water | HCID 962 | — |
| Product | Methyl 3-fluoro-11-oxo-6,7,8,9,10,11-hexahydro-5H-cyclohepta[b]quinoline-1-carboxylate | HCID 89669535 | 107.2% |
Reaction Steps
A mixture of methyl 2-oxocycloheptanecarboxylate (0.34 g, 2 mmol), methyl 3-amino-5-fluorobenzoate (0.33 g, 2 mmol), polyphosphoric acid (4.0 g) and dioxane (5 mL) was heated at 130° C. for 5 hours. After cooling to room temperature, the solution was diluted with water (100 mL), and NaOAc.3H2O (7.3 g) was added. Then the resulting precipitate was collected by filtration and dried. The solid was suspended in methanol (20 mL) and SOCl2 (10 mL) was added, the mixture was stirred at reflux for 5 hours, concentrated and treated with water (50 mL), extracted with ethyl acetate (3×50 mL). The organic layer was separated, concentrated and the residue was chromatographed to give the crude product (0.62 g). MS (ESI) m/e [M+1]+290.0.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09328111B2 |
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| Source dataset | uspto-grants-2016_05 |
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| ORD ID | ord-a937d8b4fc3f45eb803ae03ae362bce1 |
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| Source note | uspto-grants-2016_05 |
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