반응식
[CH:1]1([N:4]2[C:9]3[N:10]=[C:11]([S:15](=[S:18])([OH:17])=[O:16])[C:12]([F:14])=[CH:13][C:8]=3[C:7](=[O:19])[NH:6][C:5]2=[O:20])[CH2:3][CH2:2]1.[H-].[Na+].[N+:23](C1C=C([N+]([O-])=O)C=CC=1NO)([O-])=O>CN(C)C=O.O1CCOCC1>[NH2:23][N:6]1[C:7](=[O:19])[C:8]2[CH:13]=[C:12]([F:14])[C:11]([S:15](=[S:18])([OH:17])=[O:16])=[N:10][C:9]=2[N:4]([CH:1]2[CH2:3][CH2:2]2)[C:5]1=[O:20]참가 물질
반응물 3
생성물 1
시약·촉매·용매 1
실험 절차
A solution of 0.47 g (1.57 mmol) of 1-cyclopropyl-6-fluoro-2,4-dioxo-1,2,3,4-tetrahydro-pyrido[2,3-d]pyrimidine-7-thiosulfonic acid (Example 35) in 20 mL of dimethylformamide/dioxane (1:1) is treated portionwise with 0.08 g (2.0 mmol) of 60% sodium hydride/mineral oil. The reaction is stirred at room temperature for 1 hour and 0.32 g (1.6 mmol) of 2,4-dinitrophenylhydroxylamine is added all at once. After stirring at room temperature overnight, the dioxane is removed in vacuo and the residue is diluted to 100 mL with ice and water and stirred at 5° C. for 1 hour. The aqueous solution is extracted with ethyl acetate (3×50 mL) with the combined organic layers being washed with water, dried (MgSO4), filtered and evaporated in vacuo to give 0.4 g of the title compound, mp 167–169° C.
후처리
- stirringAfter stirring at room temperature overnight
- customthe dioxane is removed in vacuo
- additionthe residue is diluted to 100 mL with ice and water
- stirringstirred at 5° C. for 1 hour
- extractionThe aqueous solution is extracted with ethyl acetate (3×50 mL) with the combined organic layers
- washbeing washed with water
- dry with materialdried (MgSO4)
- filtrationfiltered
- customevaporated in vacuo
출처 및 근거
- ORD 기록
- ord-4df6972c6e4c48278a3fccf487f8d5a4
- 출처 데이터셋
- uspto-grants-2006_08
- 특허 번호
- US07094780B1
연결된 노트
불러오는 중…