Potassium Carbonate → 6-[(Dimethylamino)methyl]-7-hydroxy-1-(2-methoxyethyl)-N,N,2-trimethyl-1H-benzimidazole-5-carboxamide

HRID 1258465ノート

反応式

HRID 1258465 の反応式
[OH:1][C:2]1[C:7]2[N:8]([CH2:12][CH2:13][O:14][CH3:15])[C:9]([CH3:11])=[N:10][C:6]=2[CH:5]=[C:4]([C:16]([N:18]([CH3:20])[CH3:19])=[O:17])[CH:3]=1.C(=O)([O-])[O-].[K+].[K+]>CN(C)C=O>[CH3:7][N:8]([CH2:12][C:3]1[C:4]([C:16]([N:18]([CH3:20])[CH3:19])=[O:17])=[CH:5][C:6]2[N:10]=[C:9]([CH3:11])[N:8]([CH2:12][CH2:13][O:14][CH3:15])[C:7]=2[C:2]=1[OH:1])[CH3:9]

参加物

4

実験手順

To a stirred solution of 7-hydroxy-1-(2-methoxyethyl)-N,N,2-trimethyl-1H-benzimidazole-5-carboxamide (1.0 g, 3.6 mmol, Step 2) and potassium carbonate (748 mg, 5.4 mmol) in N,N-dimethylformamide (36 mL) at 0° C. was added N,N-dimethylmethyleneiminium iodide (867 mg, 4.7 mmol). After stirring at the same temperature for 4 hours, the reaction mixture was quenched with saturated sodium hydrogencarbonate aqueous solution and extracted with dichloromethane. The combined organic layer was washed with brine, dried over magnesium sulfate, and concentrated in vacuo. The residue was purified by column chromatography on NH-gel eluting with ethyl acetate/methanol (30:1) to afford the title compound (855 mg, 71%) as a white amorphous.

後処理

  1. customthe reaction mixture was quenched with saturated sodium hydrogencarbonate aqueous solution
  2. extractionextracted with dichloromethane
  3. washThe combined organic layer was washed with brine
  4. dry with materialdried over magnesium sulfate
  5. concentrationconcentrated in vacuo
  6. customThe residue was purified by column chromatography on NH-gel
  7. washeluting with ethyl acetate/methanol (30:1)

出典と根拠

ORDレコード
ord-b40c95a2048b4cc7bfbb476514732319
出典データセット
uspto-grants-2013_06
特許番号
US08466166B2

反応ノート

読み込み中…