反应详情

1.9 g of 4-benzyloxyphenylboronic acid, 1.63 g of sodium carbonate in 20 cm3 of distilled water and 500 mg of tetrakis(triphenylphosphine)palladium are added to 1.35 g of N-[5,6-dibromo-1-[[2-(trimethylsilyl)ethoxy]methyl]-1H-indazol-3-yl]butanamide, described in Example 70, in 100 cm3 of dioxane. The mixture is refluxed for 18 hours, the temperature is then allowed to return to room temperature to add 100 cm3 of ethyl acetate and 100 cm3 of water, and the reaction medium is filtered through a sinter funnel packed with Celite. The organic phase is separated out after settling of the phases has taken place, washed with 100 cm of saturated aqueous sodium chloride solution, separated out after settling of the phases has taken place, dried over magnesium sulphate, filtered and concentrated to dryness under reduced pressure (2 kPa; 50° C.). The residue is purified by chromatography under an argon pressure of 50 kPa, on a column of silica gel (particle size 40-60 μm; diameter 4.5 cm), eluting with a cyclohexane/ethyl acetate mixture (70/30 by volume). The fractions containing the expected product are combined, evaporated under reduced pressure (2 kPa; 50° C.) and dried (90 Pa; 50° C.) to give 1.96 g of N-[5,6-bis[4-(phenylmethoxy)phenyl]-1-[[2-(trimethylsilyl)ethoxy]methyl]-1H-indazol-3-yl]butanamide in the form of an orange-coloured oil in a purity of 70%, which product is used without further modification in the following step.

1. temperatureThe mixture is refluxed for 18 hours
2. customto return to room temperature
3. filtrationthe reaction medium is filtered through a sinter funnel
4. customThe organic phase is separated out
5. washwashed with 100 cm of saturated aqueous sodium chloride solution
6. customseparated out
7. dry with materialdried over magnesium sulphate
8. filtrationfiltered
9. concentrationconcentrated to dryness under reduced pressure (2 kPa; 50° C.)
10. customThe residue is purified by chromatography under an argon pressure of 50 kPa
11. washon a column of silica gel (particle size 40-60 μm; diameter 4.5 cm), eluting with a cyclohexane/ethyl acetate mixture (70/30 by volume)
12. additionThe fractions containing the expected product
13. customevaporated under reduced pressure (2 kPa; 50° C.)
14. customdried (90 Pa; 50° C.)