反应详情

To a solution of 1-[2-[5-[3, 5-di-tert-butyl-4-{(2-methoxyethoxy)methoxy}phenyl]-(2E, 4E)-2, 4-pentadienoylamino]ethyl]-4-(3-indolyl)piperidine (0.5 g) in methanol (5 ml) was added dropwise methanesulfonic acid (0.26 ml) at 18°-25° C. After 2 hours the reaction mixture was adjusted to pH 7.5 with 2N-sodium hydroxide and then poured into saturated sodium bicarbonate solution (50 ml). The resulting precipitate was collected and washed with water. The precipitate was subjected to column chromatography on silica gel and eluted with a mixture of chloroform and methanol (20:1, V/V). The fractions containing the object compound were combined and concentrated under reduced pressure. The residue was recrystallized from 1, 4-dioxane, to give white crystals of 1-[2-{5-(3, 5-di-tert-butyl-4-hydroxyphenyl)-(2E, 4E)-2, 4-pentadienoylamino}ethyl]-4-(3-indolyl)piperidine (0.28 g).

1. customThe resulting precipitate was collected
2. washwashed with water
3. washeluted with a mixture of chloroform and methanol (20:1, V/V)
4. additionThe fractions containing the object compound
5. concentrationconcentrated under reduced pressure
6. customThe residue was recrystallized from 1, 4-dioxane