Potassium Carbonate → 2-Dimethylcarbamoyl-5-methyl-octahydro-cyclopenta[c]pyrrole-5-carboxylic acid
反応式
[CH3:1][N:2]([CH3:16])[C:3]([N:5]1[CH2:9][CH:8]2[CH2:10][C:11](C#N)([CH3:13])[CH2:12][CH:7]2[CH2:6]1)=[O:4].[C:17](=[O:20])([O-])[O-:18].[K+].[K+]>Cl.O>[CH3:1][N:2]([CH3:16])[C:3]([N:5]1[CH2:9][CH:8]2[CH2:10][C:11]([CH3:13])([C:17]([OH:18])=[O:20])[CH2:12][CH:7]2[CH2:6]1)=[O:4]参加物
反応条件
- 温度
- 50 °C
実験手順
5-Cyano-5-methyl-hexahydro-cyclopenta[c]pyrrole-2-carboxylic acid dimethylamide 12b (6.99 g, 31.6 mmol) was dissolved in 90 mL of hydrochloric acid (36%). The reaction mixture was heated at 50° C. in an oil bath and stirred for 48 hours. The reaction was monitored by TLC until the disappearance of the starting materials. The reaction mixture was diluted with 100 mL of water. Upon cooling by an ice-water bath, the mixture was adjusted to pH 6 with potassium carbonate and extracted with ethy acetate (1500 mL×3) and dichloromethane (150 mL×3) successively. The combined organic extracts were dried over anhydrous sodium sulfate, filtered and concentrated under reduced pressure to obtain the title compound 2-dimethylcarbamoyl-5-methyl-octahydro-cyclopenta[c]pyrrole-5-carboxylic acid 12c (7.0 g, yield 92%) as a yellow liquid, which was directly used in the next step.
後処理
- temperatureUpon cooling by an ice-water bath
- extractionextracted with ethy acetate (1500 mL×3) and dichloromethane (150 mL×3) successively
- dry with materialThe combined organic extracts were dried over anhydrous sodium sulfate
- filtrationfiltered
- concentrationconcentrated under reduced pressure
出典と根拠
- ORDレコード
- ord-144cb36c119f4dd089e05ecd446723b5
- 出典データセット
- uspto-grants-2013_04
- 特許番号
- US08415349B2
反応ノート
読み込み中…