Dimethylformamide → 5-Bromo-1-(cyclopropylmethyl)-1,2-dihydropyridin-2-one

HRID 406739

反応式

HRID 406739 の反応式
[CH3:1][C:2]([O-])([CH3:4])[CH3:3].[K+].[Br:7][C:8]1[CH:9]=[CH:10][C:11](=[O:14])[NH:12][CH:13]=1.C1(CBr)CC1.CN(C)C=O>O1CCCC1.C(OCC)(=O)C>[Br:7][C:8]1[CH:9]=[CH:10][C:11](=[O:14])[N:12]([CH2:1][CH:2]2[CH2:4][CH2:3]2)[CH:13]=1

参加物

7

反応条件

温度
70 °C

実験手順

KOtBu (0.68 g) was added to a solution of 5-bromo-1H-pyridin-2-one (1.00 g) in tetrahydrofuran (20 mL) at room temperature. After stirring for 30 min, cyclopropylmethyl bromide (0.77 mL) and dimethylformamide (3 mL) were added to the suspension and the resulting mixture was warmed to 70° C. After stirring the mixture at 70° C. for 2 h, the reaction was complete. The mixture was cooled to room temperature, diluted with ethyl acetate (50 mL), and washed with water (2×20 mL) and brine (20 mL). Then, the solution was dried (MgSO4) and the solvent was removed to give the title compound as a colorless oil. Yield: 1.18 g (90% of theory). Mass spectrum (ESI+): m/z=228/230 (Br) [M+H]+

後処理

  1. stirringAfter stirring the mixture at 70° C. for 2 h
  2. temperatureThe mixture was cooled to room temperature
  3. washwashed with water (2×20 mL) and brine (20 mL)
  4. dry with materialThen, the solution was dried (MgSO4)
  5. customthe solvent was removed

出典と根拠

ORDレコード
ord-9bfaa689c8aa4cc797aef459d43e459a
出典データセット
uspto-grants-2014_06
特許番号
US08754076B2

関連ノート

読み込み中…