Cesium carbonate → 6-(1-Hydroxy-1,3-dihydro-benzo[c][1,2]oxaborol-5-yloxy)-5-methoxymethoxy-nicotinonitrile

HRID 1471582

反応式

HRID 1471582 の反応式
Cl[C:2]1[C:9]([O:10][CH2:11][O:12][CH3:13])=[CH:8][C:5]([C:6]#[N:7])=[CH:4][N:3]=1.[B:14]1([OH:24])[C:18]2[CH:19]=[CH:20][C:21]([OH:23])=[CH:22][C:17]=2[CH2:16][O:15]1.C(=O)([O-])[O-].[Cs+].[Cs+]>CN(C=O)C>[OH:24][B:14]1[C:18]2[CH:19]=[CH:20][C:21]([O:23][C:2]3[C:9]([O:10][CH2:11][O:12][CH3:13])=[CH:8][C:5]([C:6]#[N:7])=[CH:4][N:3]=3)=[CH:22][C:17]=2[CH2:16][O:15]1

参加物

5

反応条件

温度
80 °C

実験手順

To a mixture of 6-chloro-5-methoxymethoxy-nicotinonitrile (0.68 g, 3.42 mmol) and 3H-benzo[c][1,2]oxaborole-1,5-diol (0.56 g, 3.76 mmol) in DMF (10 mL) was added cesium carbonate (2.45 g, 7.52 mmol). The resulting suspension was heated at 80° C. for overnight. DMF was removed under reduced pressure, the residue was diluted with EtOAc (50 mL), washed with water (10 mL) and brine (10 mL), dried over Na2SO4, filtered, and concentrated to give brown oil. Purification was accomplished by flash chromatography on silica gel using 1-100% MeOH/EtOAc gradient elution to yield the title compound (0.40 g, 40%) as a transparent oil. 1H NMR (400 MHz, DMSO-d6) δ ppm 9.23 (s, 1 H), 8.24 (s, 1 H), 8.03 (s, 1 H), 7.77 (d, J=8.6 Hz, 1 H), 7.23 (s, 1 H), 7.14 (d, J=7.4 Hz, 1 H), 5.40 (s, 2 H), 4.98 (s, 2 H), 3.45 (s, 3 H); MS (ES) m/z: 313 (M+1)+.

後処理

  1. customDMF was removed under reduced pressure
  2. additionthe residue was diluted with EtOAc (50 mL)
  3. washwashed with water (10 mL) and brine (10 mL)
  4. dry with materialdried over Na2SO4
  5. filtrationfiltered
  6. concentrationconcentrated
  7. customto give brown oil
  8. customPurification
  9. washwas accomplished by flash chromatography on silica gel using 1-100% MeOH/EtOAc gradient elution

出典と根拠

ORDレコード
ord-b08f5744a62e46e8ab42a99b97edbb39
出典データセット
uspto-grants-2015_04
特許番号
US09012431B2

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