反应详情

1.05 g (4.5 mmol) of 3-bromobiphenyl and 0.9 g (3.6 mmol) of 1-(2,2-dimethylpropanoyl)-4-(1,1-dimethylprop-2-yn-1-yl)piperazine, prepared in step 5.1., 0.75 ml (5.38 mmol) of triethylamine and 0.028 g (0.11 mmol) of triphenylphosphine are dissolved in 8 ml of tetrahydrofuran. Under an argon atmosphere, 0.126 g (0.18 mmol) of the dichloride complex of bis(triphenylphosphine) palladium is added. The mixture is stirred for 15 minutes and then 0.014 g (0.07 mmol) of cuprous iodide is added. The mixture is stirred at ambient temperature for 4 hours and then at 60° C. overnight. After cooling to temperature it is diluted with 25 ml of ethyl acetate and filtered on paper. The solid is rinsed with 4 times 10 ml of ethyl acetate. 4 g of silica are added to the filtrate, which is evaporated to dryness. The residue is purified by chromatography on silica gel, eluting with a 90/10 then 80/20 and 70/30 mixture of cyclohexane and ethyl acetate, to give 0.90 g (2.22 mmol) of product in the form of a orange-colored oil.

1. stirringThe mixture is stirred at ambient temperature for 4 hours
2. customat 60° C.
3. customovernight
4. temperatureAfter cooling to temperature it
5. filtrationfiltered on paper
6. washThe solid is rinsed with 4 times 10 ml of ethyl acetate
7. addition4 g of silica are added to the filtrate, which
8. customis evaporated to dryness
9. customThe residue is purified by chromatography on silica gel
10. washeluting with a 90/10
11. addition80/20 and 70/30 mixture of cyclohexane and ethyl acetate