2,6-Lutidine → 8-Chloro-4,6-dimethyl-5-oxo-5,6-dihydrobenzo[c][2,7]naphthyridine-9-carbaldehyde
반응식
[Cl:1][C:2]1[C:3]([CH:19]=C)=[CH:4][C:5]2[C:14]3[C:9](=[C:10]([CH3:15])[N:11]=[CH:12][CH:13]=3)[C:8](=[O:16])[N:7]([CH3:17])[C:6]=2[CH:18]=1.CC1C=CC=C(C)N=1.I([O-])(=O)(=O)=[O:30].[Na+]>O1CCOCC1.O.C(OCC)(=O)C.[Os](=O)(=O)(=O)=O>[Cl:1][C:2]1[C:3]([CH:19]=[O:30])=[CH:4][C:5]2[C:14]3[C:9](=[C:10]([CH3:15])[N:11]=[CH:12][CH:13]=3)[C:8](=[O:16])[N:7]([CH3:17])[C:6]=2[CH:18]=1참가 물질
반응물 3
생성물 1
시약·촉매·용매 4
실험 절차
To a solution of 8-chloro-4,6-dimethyl-9-vinylbenzo[c][2,7]naphthyridin-5(6H)-one (600 mg, 2.107 mmol), osmium tetroxide (2.5% in 2-methyl-2-propanol) (0.794 mL, 0.063 mmol), and 2,6-dimethylpyridine (0.491 mL, 4.21 mmol) in 1,4-dioxane (30 mL) and water (30 mL) cooled to 0° C. was added sodium periodate (1803 mg, 8.43 mmol). The mixture was warmed to room temperature and stirred for 3 h. The mixture was diluted with ethyl acetate and filtered through diatomaceous earth (Celite®). The organic layer was concentrated under reduced pressure to afford a brown solid. The solid was washed with hexane (3×20 mL) and dried under vacuum to afford 8-chloro-4,6-dimethyl-5-oxo-5,6-dihydrobenzo[c][2,7]naphthyridine-9-carbaldehyde 0.6 g, 2.107 mmol, 84% yield) as a gummy brown solid. LC/MS (ESI) m/e 287.0 [(M+H)+, calcd for C15H12ClN2O2, 287.1]; LC/MS retention time (method B): tR=2.03 min.
후처리
- filtrationfiltered through diatomaceous earth (Celite®)
- concentrationThe organic layer was concentrated under reduced pressure
- customto afford a brown solid
- washThe solid was washed with hexane (3×20 mL)
- customdried under vacuum
출처 및 근거
- ORD 기록
- ord-f6d0628a54a74a81a8835de42daaa081
- 출처 데이터셋
- uspto-grants-2014_12
- 특허 번호
- US08901305B2
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