2-Butyrylamino-4-methyl-3-nitropyridine → 7-Methyl-2-propyl-1H-imidazo[4,5-b]pyridine

HRID 248369

反応式

HRID 248369 の反応式
[C:1]([NH:6][C:7]1[C:12]([N+:13]([O-])=O)=[C:11]([CH3:16])[CH:10]=[CH:9][N:8]=1)(=O)[CH2:2][CH2:3][CH3:4]>C(O)(=O)C.C(O)C.[Fe]>[CH3:16][C:11]1[CH:10]=[CH:9][N:8]=[C:7]2[NH:6][C:1]([CH2:2][CH2:3][CH3:4])=[N:13][C:12]=12

参加物

5

反応条件

温度
90 °C

実験手順

A solution of 2-butyrylamino-4-methyl-3-nitropyridine (7.0 g) and iron powder (17.5 g) in a mixture of acetic acid (14 ml) and ethanol (100 ml) was stirred at 90° C. for 3 hours under nitrogen atmosphere. After being cooled to room temperature, the reaction mixture was filtered through Celite and the filtrate was evaporated in vacuo. Ethyl acetate and saturated aqueous sodium hydrogencarbonate were added to the residue until pH 7~8 and the resulting suspension was filtered through Celite. The organic layer of the filtrate was separated, washed with brine and dried over magnesium sulfate. The solvent was evaporated in vacuo and the residue was purified with silica gel column chromatography (eluent: ethyl acetate) to give 7-methyl-2-propyl-3H-imidazo[4,5-b]pyridine (3.6 g).

後処理

  1. temperatureAfter being cooled to room temperature
  2. filtrationthe reaction mixture was filtered through Celite
  3. customthe filtrate was evaporated in vacuo
  4. additionEthyl acetate and saturated aqueous sodium hydrogencarbonate were added to the residue until pH 7~8
  5. filtrationthe resulting suspension was filtered through Celite
  6. customThe organic layer of the filtrate was separated
  7. washwashed with brine
  8. dry with materialdried over magnesium sulfate
  9. customThe solvent was evaporated in vacuo
  10. customthe residue was purified with silica gel column chromatography (eluent: ethyl acetate)

出典と根拠

ORDレコード
ord-4ea7fbf12f5f465086af47a2d5d03b9e
出典データセット
uspto-grants-1993_05
特許番号
US05210092

関連ノート

読み込み中…