Ammonia → 1,6-Naphthyridin-2-amine
반응식
Cl[C:2]1[C:11]2[C:6](=C[C:8]([NH:12]S(C3C=CC(C)=CC=3)(=O)=O)=[CH:9][CH:10]=2)[CH:5]=[CH:4][N:3]=1.[NH3:23]>>[NH2:23][C:8]1[CH:9]=[CH:10][C:11]2[C:6](=[CH:5][CH:4]=[N:3][CH:2]=2)[N:12]=1참가 물질
3
실험 절차
2-Chloro-1,6-naphthyridine (0.628 g, Production Example 22b) and an aqueous ammonia (40 ml) were heated at 130° C. for 11 hours in a sealed tube. After cooling, the mixture was extracted with ethyl acetate, and the extract was washed with brine and dried over anhydrous magnesium sulfate. The solvent was evaporated and the residue was purified by silica gel column, to give the title compound (0.497 g, 89.73%) as pale yellow crystals.
후처리
- temperatureAfter cooling
- extractionthe mixture was extracted with ethyl acetate
- washthe extract was washed with brine
- dry with materialdried over anhydrous magnesium sulfate
- customThe solvent was evaporated
- customthe residue was purified by silica gel column
출처 및 근거
- ORD 기록
- ord-b492d7e909e84a3b8aeb98ec74f19799
- 출처 데이터셋
- uspto-grants-2010_11
- 특허 번호
- US07834049B2
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