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Methanol → HCID 178521923、化合物

HRID 1887241
ノート
印刷プレビュー

反応式

HRID 1887241 の反応式
C[O:2][C:3]1[CH:4]=[C:5]([CH:15]=[CH:16][N:17]=1)[C:6]([NH:8][C:9]1[CH:14]=[CH:13][CH:12]=[CH:11][CH:10]=1)=[O:7].I[Si](C)(C)C.CO>C(Cl)(Cl)Cl>[OH:2][C:3]1[CH:4]=[C:5]([CH:15]=[CH:16][N:17]=1)[C:6]([NH:8][C:9]1[CH:14]=[CH:13][CH:12]=[CH:11][CH:10]=1)=[O:7]
参加物実験手順後処理出典と根拠反応ノート

参加物

5

反応物 3

HCID 887MethanolHCID 85247Trimethylsilyl iodideHCID 232554442-Methoxy-N-phenylpyridine-4-carboxamide

生成物 1

HCID 178521923HCID 178521923、化合物収率 37.3%

試薬・触媒・溶媒 1

HCID 6212Chloroform溶媒

実験手順

To a solution of 2-methoxy-N-phenylisonicotinamide (1.00 g, 4.38 mmol) in anhydrous chloroform (60 mL) was added iodotrimethylsilane (17.50 g, 87.50 mmol). The reaction mixture was stirred at reflux for 16 hours. After cooling to ambient temperature, methanol (10 mL) was added dropwise to quench the reaction. The solvent was removed in vacuo. The residue was dissolved in ethyl acetate (300 mL) and washed with saturated aqueous sodium bicarbonate solution (2×100 mL) and brine (150 mL). The organic layer was dried over anhydrous sodium sulfate, filtered and concentrate in vacuo. The brown crude product was recrystallised from ethyl acetate and methanol to afford the title compound as a colourless solid (0.35 g, 19%): 1H NMR (300 MHz, DMSO-d6) δ 11.88 (br s, 1H), 10.31 (s, 1H), 7.73-7.68 (m, 2H), 7.47 (d, J=6.8 Hz, 1H), 7.31 (t, J=7.9 Hz, 2H), 7.10-7.05 (m, 1H), 6.81 (s, 1H), 6.49 (dd, J=6.8, 1.7 Hz, 1H); MS (ES+) m/z 215.2 (M+1).

後処理

  1. temperatureat reflux for 16 hours
  2. customto quench
  3. customthe reaction
  4. customThe solvent was removed in vacuo
  5. dissolutionThe residue was dissolved in ethyl acetate (300 mL)
  6. washwashed with saturated aqueous sodium bicarbonate solution (2×100 mL) and brine (150 mL)
  7. dry with materialThe organic layer was dried over anhydrous sodium sulfate
  8. filtrationfiltered
  9. concentrationconcentrate in vacuo
  10. customThe brown crude product was recrystallised from ethyl acetate and methanol

出典と根拠

ORDレコード
ord-67f2605ef1904774beeec81a4577bddd
出典データセット
uspto-grants-2013_08
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US08501746B2

反応ノート

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