反应详情

1-Hydroxybenzotriazole (540 mg, 4.0 mmol), 6-(1H-indol-3-yl)hexylamine (432 mg, 2.0 mmol) and N-methylmorpholine (0.444 ml, 4.0 mmol) were added to a solution of 4-dimethylamino-4-phenylcyclohexyl-acetic acid hydrochloride (595 mg, 2.0 mmol) in dry dimethylformamide (10 ml) under argon. The clear solution was cooled in an ice-bath, dicyclohexylcarbodiimide (825 mg, 4.0 mmol) was added and the mixture was stirred at RT for 5 d, during which dicyclohexylurea precipitated out. Working up of the mixture was carried out by separating off the urea which had precipitated out and introducing the filtrate into a mixture of saturated NaCl solution (40 ml) and saturated NaHCO3 solution (10 ml). Still further urea thereby precipitated out and was separated off. After 10 min the crude product precipitated out of the filtrate and was filtered off. The aqueous phase was diluted with water (300 ml), 5 M sodium hydroxide solution (7 ml, 35 mmol) was added and the mixture was stored at 5° C. for 3 d. Further product thereby precipitated out as a beige-coloured solid in a yield of 9% (82 mg) with an m.p. of 152-156° C. The crude product was purified by chromatography on silica gel (40 g) with EA/methanol (4:1) and (1:1). The product was thereby isolated as a beige-coloured compound (534 mg) in a yield of 58%.

1. temperatureThe clear solution was cooled in an ice-bath
2. customprecipitated out
3. customby separating off the urea which
4. customhad precipitated out
5. additionintroducing the filtrate
6. additioninto a mixture of saturated NaCl solution (40 ml) and saturated NaHCO3 solution (10 ml)
7. customStill further urea thereby precipitated out and
8. customwas separated off
9. customAfter 10 min the crude product precipitated out of the filtrate
10. filtrationwas filtered off
11. additionwas added
12. customFurther product thereby precipitated out as a beige-coloured solid in a yield of 9% (82 mg) with an m.p. of 152-156° C
13. customThe crude product was purified by chromatography on silica gel (40 g) with EA/methanol (4:1) and (1:1)