反応式
[CH3:1][N:2]1[C:6](=[O:7])[C@H:5](O)[CH2:4][C@H:3]1[C:9]1[CH:14]=[CH:13][CH:12]=[N:11][CH:10]=1.C1(=O)OC(=O)CC1.N1C=CC=CC=1>CN(C)C=O>[CH3:1][N:2]1[C:6](=[O:7])[CH2:5][CH2:4][C@H:3]1[C:9]1[CH:14]=[CH:13][CH:12]=[N:11][CH:10]=1参加物
5
実験手順
Cotinine hemisuccinate was prepared by dissolving 19 mg of trans-3'-hydroxycotinine in 1 ml of dimethylformamide (Aldrich). 21 mg of succinic anhydride (Aldrich) were added, followed by 15 μl of pyridine (Aldrich). The mixture was incubated overnight at 45° C.
出典と根拠
- ORDレコード
- ord-7c2cd0ad0eb24c1c8ca3ae468fdcc9cc
- 出典データセット
- uspto-grants-1996_06
- 特許番号
- US05527686
関連ノート
読み込み中…