6-Chloronicotinoyl Chloride → 6-Chloro-N-methoxy-N-methylnicotinamide
反応式
[Cl:1][C:2]1[N:7]=[CH:6][C:5]([C:8](Cl)=[O:9])=[CH:4][CH:3]=1.ClC1C=CC(C(C2N(C)C=NC=2)=O)=CN=1.FC1N=CC(C(Cl)=O)=CC=1.FC1N=CC([C:43]([N:45]([O:47][CH3:48])C)=O)=CC=1>>[Cl:1][C:2]1[N:7]=[CH:6][C:5]([C:8]([N:45]([O:47][CH3:48])[CH3:43])=[O:9])=[CH:4][CH:3]=1参加物
5
実験手順
The title compound was prepared using 6-chloropyridine-3-carbonyl chloride (Intermediate 22, step a) in place of 6-fluoropyridine-3-carbonyl chloride according to the procedure described for Intermediate 21, step b.
出典と根拠
- ORDレコード
- ord-523d37c3c2234f9c8e902158e9a2624a
- 出典データセット
- uspto-grants-2016_04
- 特許番号
- US09309222B2
反応ノート
読み込み中…