反应详情

Oxindole (176 mg, 1.32 mmol) was dissolved in a 1:1 mixture of THF:DMF (4 mL), under N2, at RT. NaH (53 mg of a 60% suspension in mineral oil, 1.32 mmol) was added, which produced a vigorous gas evolution. This mixture was stirred for 30 min at RT, then (4-chloro-[1,3,5]triazin-2-yl)-(3,4,5-trimethoxy-phenyl)amine (156 mg, 0.53 mmol) was added and the reaction was heated to 80° C. for 2 h. The reaction was cooled to RT, partially concentrated under reduced pressure, diluted with EtOAc, then extracted with water. The water extract was back extracted two times with fresh EtOAc. All of the EtOAc extracts were washed with brine, combined, dried over NaSO4, filtered and concentrated. The recovered material was purified by preparative HPLC (5 to 100% CH3CN:H2O (0.1% TFA buffer) over 10 min at 20 mL/min) Crystals formed in the recovered eluant, which were recovered by vacuum filtration, washed with water, and dried under high vacuum giving 3-[4-(3,4,5-trimethoxy-phenylamino)-[1,3,5]triazin-2-yl]-1H-indol-2-ol as a yellow solid: MS m/z=394 [M+H]+. Calc'd for C20H19N5O4: 393.14.

1. customat RT
2. customwhich produced a vigorous gas evolution
3. temperaturethe reaction was heated to 80° C. for 2 h
4. temperatureThe reaction was cooled to RT
5. concentrationpartially concentrated under reduced pressure
6. additiondiluted with EtOAc
7. extractionextracted with water
8. extractionThe water extract
9. extractionwas back extracted two times with fresh EtOAc
10. washAll of the EtOAc extracts were washed with brine
11. dry with materialdried over NaSO4
12. filtrationfiltered
13. concentrationconcentrated
14. customThe recovered material was purified by preparative HPLC (5 to 100% CH3CN:H2O (0.1% TFA buffer) over 10 min at 20 mL/min) Crystals
15. customformed in the recovered eluant, which
16. filtrationwere recovered by vacuum filtration
17. washwashed with water
18. customdried under high vacuum