Methylamine → Methyl((1-methylpiperidin-3-yl)methyl)amine
反応式
Cl[CH2:2][CH:3]1[CH2:8][CH2:7][CH2:6][N:5]([CH3:9])[CH2:4]1.[CH3:10][NH2:11]>C(O)C>[CH3:10][NH:11][CH2:2][CH:3]1[CH2:8][CH2:7][CH2:6][N:5]([CH3:9])[CH2:4]1参加物
4
実験手順
A solution of 3-(chloromethyl)-1-methylpiperidine (9.2 g, 50 mmol) (U.S. Pat. No. 6,184,338, example 5) and 33% methylamine in ethanol (60 mL) in ethanol (30 mL) was heated in a sealed vessel at 100° C. for 17 hours. The reaction mixture was concentrated in vacuo and diluted with water before being extracted into dichloromethane and dried over magnesium sulphate. The reaction mixture was filtered and concentrated in vacuo to yield the title product, 8.2 g.
後処理
- concentrationThe reaction mixture was concentrated in vacuo
- additiondiluted with water
- extractionbefore being extracted into dichloromethane
- dry with materialdried over magnesium sulphate
- filtrationThe reaction mixture was filtered
- concentrationconcentrated in vacuo
出典と根拠
- ORDレコード
- ord-38f5bbda7a9440e8b4853f15c4b7d2a2
- 出典データセット
- uspto-grants-2007_08
- 特許番号
- US07262192B2
反応ノート
読み込み中…