2-Chloro-4-iodo-5-(trifluoromethyl)pyridine → 2-Chloro-5-(trifluoromethyl)-4-pyridinamine
反応式
[Cl:1][C:2]1[CH:7]=[C:6](I)[C:5]([C:9]([F:12])([F:11])[F:10])=[CH:4][N:3]=1.[NH3:13].CO>>[Cl:1][C:2]1[CH:7]=[C:6]([NH2:13])[C:5]([C:9]([F:12])([F:11])[F:10])=[CH:4][N:3]=1参加物
3
反応条件
- 温度
- 130 °C
実験手順
2-chloro-4-iodo-5-(trifluoromethyl)pyridine was dissolved in 7 M Ammonia/Methanol. It was heated in a Biotage Initiator microwave synthesizer at 130° C. for 1 h. A mixture of the 2- and 4-substituted products was obtained. The solvent was removed and the residue was purified by silica gel chromatography (DCM/MeOH) gradient. The pure title compound was isolated.
後処理
- additionA mixture of the 2-
- custom4-substituted products was obtained
- customThe solvent was removed
- customthe residue was purified by silica gel chromatography (DCM/MeOH) gradient
出典と根拠
- ORDレコード
- ord-9b41f0139f354fb48a2eae08892cfa9a
- 出典データセット
- uspto-grants-2013_08
- 特許番号
- US08501763B2
反応ノート
読み込み中…