Hydrochloric Acid → 1H-Indol-2-ylboronic acid

HRID 1025287

反応式

HRID 1025287 の反応式
[NH:1]1[C:9]2[C:4](=[CH:5][CH:6]=[CH:7][CH:8]=2)[CH:3]=[CH:2]1.[Li]CCCC.[B:15](OC(C)C)([O:20]C(C)C)[O:16]C(C)C.Cl.C([O-])(O)=O.[Na+]>C1COCC1>[NH:1]1[C:9]2[C:4](=[CH:5][CH:6]=[CH:7][CH:8]=2)[CH:3]=[C:2]1[B:15]([OH:20])[OH:16]

参加物

7

反応条件

温度
-40 °C

実験手順

To the SEM-protected indole prepared in step 1 (0.99 g, 4.0 mmol) in THF (10 mL) at −40° C. was added n-BuLi (2.5 M in hexanes, 1.9 mL, 4.8 mmol). The mixture was stirred at −40° C. for 1 h and then triisopropyl borate (1.2 mL, 5.2 mmol) was added. The mixture was allowed to warm to room temperature while stirring for 18 h. To the reaction mixture was added 1N HCl (aq). The mixture was stirred at room temperature for 30 minutes. The mixture was then adjusted to pH˜5 using saturated NaHCO3 (aq) The mixture was extracted with ether. The combined ether extracts were washed with water and brine, dried (Na2SO4), filtered, and concentrated in vacuo. The residue was purified by silica gel chromatography (0-50% EtOAc/hex over 30 minutes) to provide the indole boronic acid (0.20 g, 17%).

後処理

  1. temperatureto warm to room temperature
  2. stirringwhile stirring for 18 h
  3. stirringThe mixture was stirred at room temperature for 30 minutes
  4. extractionwas extracted with ether
  5. washThe combined ether extracts were washed with water and brine
  6. dry with materialdried (Na2SO4)
  7. filtrationfiltered
  8. concentrationconcentrated in vacuo
  9. customThe residue was purified by silica gel chromatography (0-50% EtOAc/hex over 30 minutes)

出典と根拠

ORDレコード
ord-a287b6ed2e6c44d996e6c6da898ea065
出典データセット
uspto-grants-2014_05
特許番号
US08729071B2

関連ノート

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