6-Chloro-3-nitropicolinamide → 3-Amino-6-chloropyridine-2-carboxamide
反応式
[Cl:1][C:2]1[N:7]=[C:6]([C:8]([NH2:10])=[O:9])[C:5]([N+:11]([O-])=O)=[CH:4][CH:3]=1>CCOC(C)=O.[Pd]>[NH2:11][C:5]1[C:6]([C:8]([NH2:10])=[O:9])=[N:7][C:2]([Cl:1])=[CH:3][CH:4]=1参加物
4
実験手順
A solution of 6-chloro-3-nitropicolinamide (0.30 g, 1.49 mmol) in EtOAc (30 mL) is hydrogenated at 60 psi over 5% Pd-C (0.10 g) for 20 min. After removal of the catalyst by filtration the solution is concentrated to dryness to give 3-amino-6-chloropicolinamide as a yellow oil, which is used directly in the next step. It is dissolved in triethylorthoformate (30 mL) and the mixture is heated under reflux for 18 h. Petroleum ether (30 mL) is added to the cooled solution, and the resulting precipitate of crude 6-chloro-3H-pyrido[3,2-d]pyrimidin-4-one (0.27 g, 99%) is filtered off and dried in a vacuum oven.
後処理
- customAfter removal of the catalyst
- filtrationby filtration the solution
- concentrationis concentrated to dryness
出典と根拠
- ORDレコード
- ord-0b55e897e8624bf6a1d9dae1c43d84f3
- 出典データセット
- uspto-grants-2004_03
- 特許番号
- US06713484B2
反応ノート
読み込み中…