Reaction #52411
ord-100ee12d0bd14ff9a03d9672a09a6d2f
Reaction equation
1-cyclopropyl-6-ethynyl-4,4-dimethyl-1,2,3,4-tetrahydro quinoline
4-[(8-cyclopropyl-3,4-dihydro-4,4-dimethylspiro[2H-1-benzopyran-2,1′-cyclopropane]-6yl)ethynyl]-2-fluoro-benzoic acid methyl ester
triethyl amine
methyl-4-iodo-phenyl acetate
4-iodo phenyl acetic acid methyl ester
Reagent B
4-iodo phenyl acetic acid methyl ester
tetrahydrofuran
Intermediate 53
4-[(8-cyclopropyl-3,4-dihydro-4,4-dimethylspiro[2H-1-benzopyran-2,1′-cyclopropane]-6yl)ethynyl]-2-fluoro-benzoic acid methyl ester
→
Reactants
1-cyclopropyl-6-ethynyl-4,4-dimethyl-1,2,3,4-tetrahydro quinoline
4-[(8-cyclopropyl-3,4-dihydro-4,4-dimethylspiro[2H-1-benzopyran-2,1′-cyclopropane]-6yl)ethynyl]-2-fluoro-benzoic acid methyl ester
triethyl amine
methyl-4-iodo-phenyl acetate
4-iodo phenyl acetic acid methyl ester
Reagent B
4-iodo phenyl acetic acid methyl ester
tetrahydrofuran
Intermediate 53
4-[(8-cyclopropyl-3,4-dihydro-4,4-dimethylspiro[2H-1-benzopyran-2,1′-cyclopropane]-6yl)ethynyl]-2-fluoro-benzoic acid methyl ester
Solvents
Conditions
Detailed conditions
See reaction.notes.procedure_details.
Procedure
Following general procedure F and using 1-cyclopropyl-6-ethynyl-4,4-dimethyl-1,2,3,4-tetrahydro quinoline (Intermediate 53, 0.05 g, 0.22 mmol), methyl-4-iodo-phenyl acetate (Reagent B, 0.055 g, 0.2 mmol), triethyl amine (5 mL), tetrahydrofuran, copper(I)iodide(0.025 g, 0.13 mmol) and dichlorobis(triphenylphosphine)palladium(II) (0.75 g, 0.11 mmol) followed preparative normal phase HPLC using 10% ethyl acetate in hexane as the mobile phase, the title compound was obtained (0.089 g, 100%).