反应详情

Under argon, 35 mg (0.13 mmol) of 1,4,7,10,13,16-hexaoxacyclooctadecane (18-crown-6) are initially charged in 7 ml of THF, and 1.98 ml (1.98 mmol) of a 1-molar potassium tert-butoxide solution in THF and 400 mg (1.32 mmol) of ethyl 5-[(3,3-dimethylbutanoyl)amino]-1H-indole-2-carboxylate from Example LXII are added. The mixture is stirred at RT for 15 minutes and cooled to 0° C. A solution of 474 mg (1.98 mmol) of 2-trifluoromethylbenzyl bromide in 12 ml of THF is slowly added dropwise. The ice-bath is removed and the mixture stirred at RT for 1 hour. For work-up, the mixture is diluted with water and the THF is removed under reduced pressure using a rotary evaporator. The aqueous residue is extracted with ethyl acetate and the organic phase is washed with sat. sodium chloride solution, dried with sodium sulphate, filtered and dried under reduced pressure. The residue is purified by column chromatography (mobile phase: cyclohexane:ethyl acetate 5:1).

1. temperaturecooled to 0° C
2. customThe ice-bath is removed
3. stirringthe mixture stirred at RT for 1 hour
4. additionFor work-up, the mixture is diluted with water
5. customthe THF is removed under reduced pressure
6. customa rotary evaporator
7. extractionThe aqueous residue is extracted with ethyl acetate
8. washthe organic phase is washed with sat. sodium chloride solution
9. dry with materialdried with sodium sulphate
10. filtrationfiltered
11. customdried under reduced pressure
12. customThe residue is purified by column chromatography (mobile phase: cyclohexane:ethyl acetate 5:1)