反应详情

A solution of 1-methyl-3-[1-(toluene-4-sulfonyl)-1H-pyrrolo[2,3-b]pyridin-2-yl]-1H-indol-5-ol [2.1 g, Reference Example 14(a)] in dry dimethylformamide (50 mL) was treated with potassium tert-butoxide (620 mg) at 0° C. under nitrogen. After stirring for 10 minutes the mixture was treated with allyl bromide (480 μl) and then allowed to warm slowly to ambient temperature. Stirring was continued for a further 6 hours after which time the mixture was poured carefully into water and the aqueous phase extracted exhaustively with ethyl acetate. The combined organic extracts were washed twice with brine (100 mL), then dried over sodium sulfate and then evaporated. The residue was subjected to flash column chromatography on silica eluting with a mixture of ethyl acetate and pentane (1:1, v/v) to give the title compound (1.2 g) as a yellow foam, m.p. 257–259° C. MS: 458(MH+).

1. stirringStirring
2. waitwas continued for a further 6 hours
3. extractionthe aqueous phase extracted exhaustively with ethyl acetate
4. washThe combined organic extracts were washed twice with brine (100 mL)
5. dry with materialdried over sodium sulfate
6. customevaporated
7. additionThe residue was subjected to flash column chromatography on silica eluting with a mixture of ethyl acetate and pentane (1:1