反应详情

A solution of 4-[1-ethyl-4-(1H-pyrrolo[2,3-b]pyridin-4-yl)-1H-pyrazol-3-yl]aniline (0.23 mmol) in tetrahydrofuran (1 mL) was treated with triethylamine (0.23 mmol) and 4-nitrophenyl chloroformate (0.23 mmol). The reaction stirred for 1 h at room temperature and was then treated with 3-biphenylamine (5 eq). After stirring 18 h at room temperature the reaction was poured into water (1 mL), and extracted with (3×1 mL) ethyl acetate. The combined organic layers were washed with 1N sodium hydroxide (3×1 mL), brine (1×1 mL), dried over sodium sulfate and concentrated in vacuo. Purification of the residue by Gilson reverse phase HPLC provided the title product as a white powder (45%). ESMS [M+H]+: 499.2

1. stirringAfter stirring 18 h at room temperature the reaction
2. extractionextracted with (3×1 mL) ethyl acetate
3. washThe combined organic layers were washed with 1N sodium hydroxide (3×1 mL), brine (1×1 mL)
4. dry with materialdried over sodium sulfate
5. concentrationconcentrated in vacuo
6. customPurification of the residue by Gilson reverse phase HPLC