반응식
FC1C=C(F)C=CC=1C1C=C(COS(C)(=O)=O)C(=O)N(CC(C)C)N=1.[F:26][C:27]1[CH:28]=[C:29]([CH:51]=[CH:52][C:53]=1[F:54])[CH2:30][N:31]1[C:36](=[O:37])[C:35]([C:38]([O:40]C)=[O:39])=[CH:34][C:33]([C:42]2[CH:47]=[CH:46][C:45]([O:48][CH3:49])=[C:44]([F:50])[CH:43]=2)=[N:32]1>>[C:38]([C:35]1[C:36](=[O:37])[N:31]([CH2:30][C:29]2[CH:51]=[CH:52][C:53]([F:54])=[C:27]([F:26])[CH:28]=2)[N:32]=[C:33]([C:42]2[CH:47]=[CH:46][C:45]([O:48][CH3:49])=[C:44]([F:50])[CH:43]=2)[CH:34]=1)([OH:40])=[O:39]참가 물질
3
반응물 2
생성물 1
실험 절차
Following the procedure of Example 1 (7), 2-(3,4-difluorobenzyl)-6-(3-fluoro-4-methoxyphenyl)-4-methoxycarbonyl-2H-pyridazin-3-one was reacted to yield the title compound as a yellow crystalline powder (yield: 97.6%).
후처리
- customwas reacted
출처 및 근거
- ORD 기록
- ord-fd0da7479f3c4910bc9f48780c1874b2
- 출처 데이터셋
- uspto-grants-2006_08
- 특허 번호
- US07087606B2
연결된 노트
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