反応 #156396

ord-5cd51a8be23c463a9f17128af014d851

反応方程式

Ic1cn[nH]c1
4-iodopyrazole
O=C([O-])[O-].[Cs+].[Cs+]
cesium carbonate
BrCCOC1CCCCO1
2-(2-bromoethoxy)tetrahydro-2H-pyran
Ic1cnn(CCOC2CCCCO2)c1
title compound
Ic1cnn(CCOC2CCCCO2)c1
4-Iodo-1-[2-(tetrahydro-pyran-2-yloxy)-ethyl]-1H-pyrazole

溶媒

反応条件

詳細条件
See reaction.notes.procedure_details.

後処理

  1. 1
    温度heating at 70° C. for 17 h
  2. 2
    その他Then the RM was quenched with 100 mL water
  3. 3
    抽出extracted with 3×120 mL EtOAc
  4. 4
    洗浄The combined organic layers were washed with 3×100 mL water and 1×100 mL brine
  5. 5
    乾燥before being dried over Na2SO4
  6. 6
    ろ過filtered
  7. 7
    その他evaporated to dryness
  8. 8
    その他The residue was purified by flash chromatography (6×25 cm, Hexane/EtOAc 0%-30%)

実験手順

In flask were introduced 4-iodopyrazole (10 g, 51.6 mmol), cesium carbonate (20.16 g, 61.9 mmol) and anhydrous DMF (98 mL). The suspension was stirred at rt for 5 min, before adding 2-(2-bromoethoxy)tetrahydro-2H-pyran (9.74 mL, 61.9 mmol) and heating at 70° C. for 17 h. Then the RM was quenched with 100 mL water and extracted with 3×120 mL EtOAc. The combined organic layers were washed with 3×100 mL water and 1×100 mL brine, before being dried over Na2SO4, filtered and evaporated to dryness. The residue was purified by flash chromatography (6×25 cm, Hexane/EtOAc 0%-30%) to afford the title compound as a colorless oil (tR 3.12 min (conditions 8), MH+=323).

出典

DOI: 10.6084/m9.figshare.5104873.v1特許: US08822468B2uspto-grants-2014_09