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Phosphorus oxychloride → 2-Chloro-7-(1-ethylpropyl)-4-methoxy-1-methyl-1H-benzimidazole

HRID 1698561
ノート
印刷プレビュー

反応式

HRID 1698561 の反応式
[CH2:1]([CH:3]([C:6]1[C:11]2[N:12]([CH3:16])[C:13](=O)[NH:14][C:10]=2[C:9]([O:17][CH3:18])=[CH:8][CH:7]=1)[CH2:4][CH3:5])[CH3:2].P(Cl)(Cl)([Cl:21])=O>>[Cl:21][C:13]1[N:12]([CH3:16])[C:11]2[C:6]([CH:3]([CH2:4][CH3:5])[CH2:1][CH3:2])=[CH:7][CH:8]=[C:9]([O:17][CH3:18])[C:10]=2[N:14]=1
参加物反応条件実験手順後処理出典と根拠反応ノート

参加物

3

反応物 2

HCID 24813Phosphorus oxychlorideHCID 672729917-(1-Ethylpropyl)-4-methoxy-1-methyl-1,3-dihydro-2H-benzimidazol-2-one

生成物 1

HCID 672730962-Chloro-7-(1-ethylpropyl)-4-methoxy-1-methyl-1H-benzimidazole収率 60%

反応条件

温度
110 °C

実験手順

A mixture of 7-(1-ethylpropyl)-4-methoxy-1-methyl-1,3-dihydro-2H-benzimidazol-2-one (190 mg, 0.765 mmol) in phosphorous oxychloride (2.14 mL) was stirred at 110° C. for 6 h. The reaction was allowed to cool to room temperature and concentrated in vacuo. The residue was dissolved in ethyl acetate and washed with aqueous sodium bicarbonate and brine. The organic layer was dried over magnesium sulfate, filtered, and concentrated in vacuo. The residue was purified by column chromatography on silica gel (n-hexane/ethyl acetate 10:1-1:1) and crystallized from ethyl acetate/n-hexane to afford the title compound as colorless crystals (123 mg, 60%).

後処理

  1. temperatureto cool to room temperature
  2. concentrationconcentrated in vacuo
  3. dissolutionThe residue was dissolved in ethyl acetate
  4. washwashed with aqueous sodium bicarbonate and brine
  5. dry with materialThe organic layer was dried over magnesium sulfate
  6. filtrationfiltered
  7. concentrationconcentrated in vacuo
  8. customThe residue was purified by column chromatography on silica gel (n-hexane/ethyl acetate 10:1-1:1)
  9. customcrystallized from ethyl acetate/n-hexane

出典と根拠

ORDレコード
ord-051f5c5729ba4a7594f3af1c0fe654fd
出典データセット
uspto-grants-2012_04
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US08163935B2

反応ノート

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