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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

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1,4-DioxaneHCID 31275—
ReactantMethyl 2-oxocycloheptane-1-carboxylateHCID 288225—
ReactantMethyl 3-amino-5-fluorobenzoateHCID 3807862—
SolventWaterHCID 962—
ProductMethyl 3-fluoro-11-oxo-6,7,8,9,10,11-hexahydro-5H-cyclohepta[b]quinoline-1-carboxylateHCID 89669535107.2%

Reaction Conditions

Temperature130 °C

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09328111B2
Source datasetuspto-grants-2016_05
ORD IDord-a937d8b4fc3f45eb803ae03ae362bce1
Source noteuspto-grants-2016_05