反応 #1140289

ord-857e91c944c249a7a5d64dec31da94a0

反応条件

温度
100°CELSIUS
詳細条件
See reaction.notes.procedure_details.

後処理

  1. 1
    その他The reaction mixture was degassed with argon for 20 min
  2. 2
    抽出extracted with ethyl acetate (2×150 mL) and organic layer
  3. 3
    洗浄was washed with brine
  4. 4
    乾燥dried over anhydrous sodium sulphate
  5. 5
    濃縮concentrated under reduced pressure
  6. 6
    その他to get crude compound
  7. 7
    その他Crude compound was purified by column chromatography
  8. 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.

出典

DOI: 10.6084/m9.figshare.5104873.v1特許: US09393248B1uspto-grants-2016_07