反応式
[Cl:1][C:2]1[N:7]=[C:6]([N:8](C)[CH3:9])[C:5]([N+:11]([O-:13])=[O:12])=[CH:4][CH:3]=1.CN>>[Cl:1][C:2]1[N:7]=[C:6]([NH:8][CH3:9])[C:5]([N+:11]([O-:13])=[O:12])=[CH:4][CH:3]=1参加物
3
実験手順
6-chloro-2-methylamino-3-nitro-pyridine was prepared in accordance to the procedure described above for the preparation of 6-chloro-2-dimethylamino-3-nitro pyridine by using solution of methyl amine. The crude product was purified by flash chromatography, eluting with 90% hexane: 10% ethyl acetate to 16 (300 mg).
後処理
- customThe crude product was purified by flash chromatography
- washeluting with 90% hexane
出典と根拠
- ORDレコード
- ord-28a6a2630152406486bf79fccdaebfea
- 出典データセット
- uspto-grants-2008_09
- 特許番号
- US07425557B2
関連ノート
読み込み中…