반응식
[OH:1][C:2]1[CH:9]=[CH:8][CH:7]=[CH:6][C:3]=1[C:4]#[N:5].C(=O)([O-])[O-].[K+].[K+].CN1CCCC1=O.F[C:24]1[C:25]([O:34][C:35]2[CH:36]=[N:37][C:38]([S:41]([CH3:44])(=[O:43])=[O:42])=[CH:39][CH:40]=2)=[CH:26][C:27]([N+:31]([O-:33])=[O:32])=[C:28]([NH2:30])[CH:29]=1>O>[C:4]([C:3]1[CH:6]=[CH:7][CH:8]=[CH:9][C:2]=1[O:1][C:24]1[C:25]([O:34][C:35]2[CH:36]=[N:37][C:38]([S:41]([CH3:44])(=[O:42])=[O:43])=[CH:39][CH:40]=2)=[CH:26][C:27]([N+:31]([O-:33])=[O:32])=[C:28]([NH2:30])[CH:29]=1)#[N:5]참가 물질
6
반응 조건
- 온도
- 90 °C
실험 절차
60 mg of 2-hydroxy-benzonitrile and 70 mg of potassium carbonate were added to an N-methylpyrrolidinone (2 ml) solution of 150 mg of 5-fluoro-4-(6-methanesulfonyl-pyridin-3-yloxy)-2-nitro-phenylamine obtained in (step 3), and the reaction liquid was stirred at 90° C. for 5 hours. Water was added to the reaction liquid, and the deposit was taken out through filtration to obtain the entitled compound.
후처리
- customobtained in (step 3)
- customthe reaction liquid
- filtrationthe deposit was taken out through filtration
- customto obtain the entitled compound
출처 및 근거
- ORD 기록
- ord-2db017ca3f4142d080bb5cc0e86c3cf0
- 출처 데이터셋
- uspto-grants-2010_06
- 특허 번호
- US07728025B2
연결된 노트
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