반응식
CCN(C(C)C)C(C)C.[F:10][C:11]([F:28])([F:27])[O:12][C:13]1[CH:14]=[CH:15][CH:16]=[C:17]2[C:22]=1[O:21][C:20](=[O:23])[C:19]([C:24]([OH:26])=O)=[CH:18]2.CN(C(ON1N=NC2C=CC=NC1=2)=[N+](C)C)C.F[P-](F)(F)(F)(F)F.[CH3:53][O:54][C:55]1[CH:60]=[CH:59][C:58]([C:61]2[CH:66]=[CH:65][CH:64]=[C:63]([NH2:67])[CH:62]=2)=[CH:57][CH:56]=1>CN(C=O)C>[CH3:53][O:54][C:55]1[CH:56]=[CH:57][C:58]([C:61]2[CH:66]=[CH:65][CH:64]=[C:63]([NH:67][C:24]([C:19]3[C:20](=[O:23])[O:21][C:22]4[C:17]([CH:18]=3)=[CH:16][CH:15]=[CH:14][C:13]=4[O:12][C:11]([F:10])([F:28])[F:27])=[O:26])[CH:62]=2)=[CH:59][CH:60]=1참가 물질
6
반응물 4
생성물 1
시약·촉매·용매 1
실험 절차
DIEA (0.0144 mL, 0.083 mmol) was added to 8-trifluoromethoxy-3-carboxy-coumarin (0.021 g, 0.075 mmol) and HATU (0.032 g, 0.083 mmol) in 0.36 mL of DMF with constant stirring at room temperature until a clear solution resulted. Subsequently, 4′-Methoxy-biphenyl-3-ylamine (0.015 g, 0.075 mmol) was added and allowed to react overnight when a solid precipitated out of solution. The resulting precipitate was filtered, dried under suction, and finally dried overnight in vacuo to give 0.019 g of product in 55% yield: LCMS (ESI) m/z 456 (MH+).
후처리
- customresulted
- customto react overnight when a solid
- customprecipitated out of solution
- filtrationThe resulting precipitate was filtered
- customdried under suction, and finally dried overnight in vacuo
출처 및 근거
- ORD 기록
- ord-4cfa2ae74b664fce945c82dfd71906e8
- 출처 데이터셋
- uspto-grants-2014_02
- 특허 번호
- US08642788B2
연결된 노트
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