6-Chloro-3-nitropicolinamide → 3-Amino-6-chloropyridine-2-carboxamide
반응식
[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]=1참가 물질
4
실험 절차
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.
후처리
- customAfter removal of the catalyst
- filtrationby filtration the solution
- concentrationis concentrated to dryness
출처 및 근거
- ORD 기록
- ord-0b55e897e8624bf6a1d9dae1c43d84f3
- 출처 데이터셋
- uspto-grants-2004_03
- 특허 번호
- US06713484B2
반응 노트
불러오는 중…