Hydrochloric Acid → HCID 66779008, compound

Participants

Reaction Conditions

Reaction Steps

To a mixture of 2-[chloro(cyclohexyl)methyl]-5-fluoro-3-methyl-1-benzofuran (1.44 g) synthesized in Example A37(3), methyl 4-aminobenzoate (776 mg), sodium iodide (1.54 g) and N,N-dimethylformamide (30 mL) was added sodium carbonate (1.09 g), and the mixture was stirred at 80° C. overnight. 1N Hydrochloric acid was added to quench the reaction, and the mixture was extracted with ethyl acetate. The extract was washed with saturated brine, dried over magnesium sulfate, and concentrated under reduced pressure. The residue was purified by silica gel column chromatography (20% ethyl acetate/hexane) to give a yellow solid. To a mixture of the obtained solid, tetrahydrofuran (20 mL) and ethanol (20 mL) was added 1N aqueous sodium hydroxide solution (20 mL), and the mixture was stirred overnight with heating under reflux, and concentrated under reduced pressure. The residue was dissolved in water (40 mL), and 1N hydrochloric acid (20 mL) was added at 0° C. The resulting precipitate was collected by filtration to give the title object compound (1.06 g, 54%) as a yellow solid.

Provenance & Evidence