Water → 3-(2-Fluorophenyl)-6-(2-Methyl-2H-1,2,4-Triazol-3-Ylmethoxy)-7-(3-Oxocyclobutyl)-1,2,4-Triazolo[4,3-b]Pyridazine
반응식
[Cr](O)(O)(=O)=O.[F:6][C:7]1[CH:12]=[CH:11][CH:10]=[CH:9][C:8]=1[C:13]1[N:17]2[NH:18][C:19](=[O:27])[C:20]([CH:22]3[CH2:25][CH:24]([OH:26])[CH2:23]3)=[CH:21][C:16]2=[N:15][N:14]=1.[CH:28](O)([CH3:30])C.O>CC(C)=O>[F:6][C:7]1[CH:12]=[CH:11][CH:10]=[CH:9][C:8]=1[C:13]1[N:17]2[N:18]=[C:19]([O:27][CH2:30][C:28]3[N:15]([CH3:16])[N:14]=[CH:13][N:17]=3)[C:20]([CH:22]3[CH2:23][C:24](=[O:26])[CH2:25]3)=[CH:21][C:16]2=[N:15][N:14]=1참가 물질
반응물 4
생성물 1
시약·촉매·용매 1
실험 절차
8N Chromic acid was added to a solution of 3-(2-fluorophenyl)-7-(3-hydroxycyclobutyl)-1,2,4-triazolo[4,3-b]pyridazin-6-one (0.36 g, 1.2 mmol) in acetone (50 ml) dropwise, until excess was present (red colour remained). The reaction was then stirred for 2 hours before isopropanol was added until the blue colour remained and no excess chromic acid was present. Water (50 ml) was added and the aqueous layer extracted with ethyl acetate (4×50 ml), organic layers were combined, washed with brine (50 ml), dried (MgSO4), filtered and concentrated to give the desired product as a white solid. Data for the title compound: 1H NMR (360 MHz, DMSO) δ3.41 (2H, s), 3.43 (2H, s), 3.73-3.78 (1H, m), 7.42-7.50 (2H, m), 7.64-7.72 (1H, m), 7.83-7.88 (1H, m), 8.38 (1H, s); MS (ES+) m/e 299 [MH]+.
후처리
- additionwas added until the blue colour
- extractionthe aqueous layer extracted with ethyl acetate (4×50 ml), organic layers
- washwashed with brine (50 ml)
- dry with materialdried (MgSO4)
- filtrationfiltered
- concentrationconcentrated
출처 및 근거
- ORD 기록
- ord-ed0ed63cae094c69a1a0a46b18685bf8
- 출처 데이터셋
- uspto-grants-2003_06
- 특허 번호
- US06579875B1
반응 노트
불러오는 중…