Methylamine → N-(2-Methoxyphenyl)-4-(methylamino)methylbenzamide

HRID 2455

反応式

HRID 2455 の反応式
Cl[CH2:2][C:3]1[CH:19]=[CH:18][C:6]([C:7]([NH:9][C:10]2[CH:15]=[CH:14][CH:13]=[CH:12][C:11]=2[O:16][CH3:17])=[O:8])=[CH:5][CH:4]=1.[CH3:20][NH2:21]>O1CCOCC1>[CH3:17][O:16][C:11]1[CH:12]=[CH:13][CH:14]=[CH:15][C:10]=1[NH:9][C:7](=[O:8])[C:6]1[CH:18]=[CH:19][C:3]([CH2:2][NH:21][CH3:20])=[CH:4][CH:5]=1

参加物

4

実験手順

4-Chloromethyl-N-(2-methoxyphenyl)benzamide (400 mg, 1.45 mmol) was dissolved in dioxane (4 ml) and then mixed with 50% methylamine aqueous solution (4 ml) at room temperature. After 1 hour of stirring at the same temperature, dioxane was removed by evaporation, and the resulting residue was diluted with methylene chloride (10 ml). After drying on anhydrous sodium carbonate, the solvent was removed by evaporation to obtain 500 mg (100%) of the title compound in the form of colorless oil.

後処理

  1. customwas removed by evaporation
  2. additionthe resulting residue was diluted with methylene chloride (10 ml)
  3. dry with materialAfter drying on anhydrous sodium carbonate
  4. customthe solvent was removed by evaporation

出典と根拠

ORDレコード
ord-1e483b3adf244fe28b89df6ce80d81bc
出典データセット
uspto-grants-1998_03
特許番号
US05728835

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