3-{2-Chloro-4-fluoro-5-[3-methyl-2,6-dioxo-4-(trifluoromethyl)-1,2,3,6-tetrahydropyrimidin-1-yl]phenoxy}-2-(benzyloxycarbonyl)methoxypyridine → 3-{2-Chloro-4-fluoro-5-[3-methyl-2,6-dioxo-4-(trifluoromethyl)-1,2,3,6-tetrahydropyrimidin-1-yl]phenoxy}-2-carboxymethoxypyridine
반응식
[Cl:1][C:2]1[CH:26]=[C:25]([F:27])[C:24]([N:28]2[C:33](=[O:34])[CH:32]=[C:31]([C:35]([F:38])([F:37])[F:36])[N:30]([CH3:39])[C:29]2=[O:40])=[CH:23][C:3]=1[O:4][C:5]1[C:6]([O:11][CH2:12][C:13]([O:15]CC2C=CC=CC=2)=[O:14])=[N:7][CH:8]=[CH:9][CH:10]=1>[Pd].C(OCC)(=O)C>[Cl:1][C:2]1[CH:26]=[C:25]([F:27])[C:24]([N:28]2[C:33](=[O:34])[CH:32]=[C:31]([C:35]([F:38])([F:37])[F:36])[N:30]([CH3:39])[C:29]2=[O:40])=[CH:23][C:3]=1[O:4][C:5]1[C:6]([O:11][CH2:12][C:13]([OH:15])=[O:14])=[N:7][CH:8]=[CH:9][CH:10]=1참가 물질
4
반응물 1
생성물 1
시약·촉매·용매 2
실험 절차
A mixture of 0.24 g of 3-{2-chloro-4-fluoro-5-[3-methyl-2,6-dioxo-4-(trifluoromethyl)-1,2,3,6-tetrahydropyrimidin-1-yl]phenoxy}-2-(benzyloxycarbonyl)methoxypyridine [present compound 7-82], 10 mg of 10% palladium/carbon and 1 ml of ethyl acetate was stirred for 1.5 hours at room temperature under hydrogen atmosphere. There action system was purged with nitrogen, then, the reaction solution was filtrated through Celite, and the filtrate was concentrated. The residue was subjected to silica gel column chromatography to obtain 0.16 g of 3-{2-chloro-4-fluoro-5-[3-methyl-2,6-dioxo-4-(trifluoromethyl)-1,2,3,6-tetrahydropyrimidin-1-yl]phenoxy}-2-carboxymethoxypyridine [present compound 7-6].
후처리
- customThere action system was purged with nitrogen
- filtrationthe reaction solution was filtrated through Celite
- concentrationthe filtrate was concentrated
출처 및 근거
- ORD 기록
- ord-266f8842f152498c9b77cf8fd1a8d0f7
- 출처 데이터셋
- uspto-grants-2003_03
- 특허 번호
- US06537948B1
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