Isopropylamine → 2-bromo-N-isopropyl-5-nitropyridin-4-amine
반응식
[CH:1]([NH2:4])([CH3:3])[CH3:2].[Br:5][C:6]1[CH:11]=[C:10](Br)[C:9]([N+:13]([O-:15])=[O:14])=[CH:8][N:7]=1>C1COCC1.O>[Br:5][C:6]1[CH:11]=[C:10]([NH:4][CH:1]([CH3:3])[CH3:2])[C:9]([N+:13]([O-:15])=[O:14])=[CH:8][N:7]=1참가 물질
5
실험 절차
A solution of isopropylamine (17 ml, 34.0 mmol) in THF (14 ml) was added dropwise over 1 h to a mixture of 2,4-dibromo-5-nitropyridine (4.94 g, 17.0 mmol) in THF (85 ml) at room temperature. After 5.5 h, the reaction mixture was diluted with H2O and extracted with EtOAc (3×). The combined organic layers were dried over Na2SO4 and evaporated to give the crude title compound as a yellow solid. (UPLC-MS 6) tR 1.03; ESI-MS 260.0/262.0 [M+H]+.
후처리
- extractionextracted with EtOAc (3×)
- dry with materialThe combined organic layers were dried over Na2SO4
- customevaporated
출처 및 근거
- ORD 기록
- ord-e8d4f605efee425e8786c56e8325d032
- 출처 데이터셋
- uspto-grants-2016_02
- 특허 번호
- US09266883B2
반응 노트
불러오는 중…