反应详情

温度

-20 °C

5-Chloro-3-iodo-1-triisopropylsilanyl-1H-pyrrolo[2,3-b]pyridine (629, 0.19 g, 0.44 mmol) was dissolved in tetrahydrofuran (0.9 mL). The solution was, cooled to −20° C. 2M isopropylmagnesium chloride in tetrahydrofuran (200 μL) was added dropwise to the mixture, then stirred to −5° C. After the reaction was cooled to −20° C., 5-(3-chloro-benzylamino)-2-methyl-2 H-pyrazole-3-carbaldehyde (648, 0.050 g, 0.20 mmol) in 2 mL of tetra.hydrofuran was added at once to the mixture. The reaction was stirred to 0° C. and then concentrated. Ethyl acetate was added and the mixture was washed with sodium bicarbonate saturated solution and brine. The organic portion was dried over anhydrous sodium sulfate and concentrated. Purification with silica gel column chromatography eluting with a gradient of ethyl acetate (5-80%) in hlexane gave the desired compound (649, 0.033 g, 30%). (ESI) [M+H+]+=558.3, 560.9.

1. temperatureAfter the reaction was cooled to −20° C.
2. stirringThe reaction was stirred to 0° C.
3. concentrationconcentrated
4. additionEthyl acetate was added
5. washthe mixture was washed with sodium bicarbonate saturated solution and brine
6. dry with materialThe organic portion was dried over anhydrous sodium sulfate
7. concentrationconcentrated
8. customPurification with silica gel column chromatography
9. washeluting with a gradient of ethyl acetate (5-80%) in hlexane