反応式
C[O:2][C:3]1[CH:8]=[C:7]([CH2:9][NH2:10])[CH:6]=[CH:5][N:4]=1>Cl>[NH2:10][CH2:9][C:7]1[CH:6]=[CH:5][NH:4][C:3](=[O:2])[CH:8]=1参加物
3
実験手順
The starting material (2-methoxypyridin-4-yl)methanamine 56-2 in 3N HCl was refluxed at 110° C. for 12 hours. The reaction was taken to dryness by rotary evaporation to give crude 4-(aminomethyl)pyridin-2(1H)-one 56-3.
後処理
- customThe reaction was taken to dryness by rotary evaporation
出典と根拠
- ORDレコード
- ord-0a0113fcf18d4c1b932891df2d2f6d59
- 出典データセット
- uspto-grants-2015_11
- 特許番号
- US09181235B2
関連ノート
読み込み中…