Dimethylamine → 6-((Dimethylamino)methyl)-3-pyridinecarboxylic acid
反応式
Br[CH2:2][C:3]1[CH:11]=[CH:10][C:6]([C:7]([OH:9])=[O:8])=[CH:5][N:4]=1.[CH3:12][NH:13][CH3:14]>CCO>[NH3:4].[CH3:12][N:13]([CH2:2][C:3]1[CH:11]=[CH:10][C:6]([C:7]([OH:9])=[O:8])=[CH:5][N:4]=1)[CH3:14]参加物
5
実験手順
2nd step: To a stirred solution of 6-bromomethyl-nicotinic acid (350 mg, 1.62 mmol) in EtOH (3 mL) was added a solution of dimethyl-amine in EtOH (2 mL, 30% solution). Stirring was continued for 1 hour, concentrated under vacuo. Column chromatography (SiO2, CH2Cl2/MeOH: 8/2, aq. NH3 1%) yielded 205 mg (70%) of 6-dimethylaminomethyl-nicotinic acid as a light brown solid. ES-MS m/e: 181.1 (M+H+).
後処理
- concentrationconcentrated under vacuo
出典と根拠
- ORDレコード
- ord-e3254bb8d29d4baaaaec976878d6975a
- 出典データセット
- uspto-grants-2011_09
- 特許番号
- US08012998B2
反応ノート
読み込み中…