反応 #1140289
ord-857e91c944c249a7a5d64dec31da94a0
反応方程式
反応物
反応条件
後処理
- 1その他The reaction mixture was degassed with argon for 20 min
- 2抽出extracted with ethyl acetate (2×150 mL) and organic layer
- 3洗浄was washed with brine
- 4乾燥dried over anhydrous sodium sulphate
- 5濃縮concentrated under reduced pressure
- 6その他to get crude compound
- 7その他Crude compound was purified by column chromatography
- 8洗浄eluted with 60% ethyl acetate in petroleum ether
実験手順
To a solution of 4-[5-(2-amino-5-bromo-pyridin-3-yl)-[1,3,4]oxadiazol-2-yl]-piperidine-1-carboxylic acid tert-butyl ester (1.1 g, 2.59 mmol) in dioxane (20 mL) and water (10 mL) were added K2CO3 (1.07 g, 7.77 mmol) and N-methylindole-5-boronic acid (0.50 g, 2.85 mmol) in a sealed tube. The reaction mixture was degassed with argon for 20 min, then Pd(PPh3)4 (0.15 g, 0.13 mmol) was added to the reaction mixture. The reaction mixture was stirred for 18 h at 100° C. The reaction was diluted with water (100 mL), extracted with ethyl acetate (2×150 mL) and organic layer was washed with brine, dried over anhydrous sodium sulphate and concentrated under reduced pressure to get crude compound. Crude compound was purified by column chromatography using 100-200 mesh silica gel compound eluted with 60% ethyl acetate in petroleum ether to afford 900 mg of the title compound which is further purified by washing with 20% chloroform in hexane to afford the title compound as a pale yellow solid.