반응식
[CH2:1]([O:5][C:6]1[CH:14]=[C:13]([O:15][CH3:16])[CH:12]=[CH:11][C:7]=1[C:8]([OH:10])=O)[CH2:2][CH2:3][CH3:4].[NH2:17][C:18]1[CH:34]=[CH:33][CH:32]=[CH:31][C:19]=1[C:20]([NH:22][C:23]1[CH:28]=[CH:27][C:26]([O:29][CH3:30])=[CH:25][CH:24]=1)=[O:21]>>[CH2:1]([O:5][C:6]1[CH:14]=[C:13]([O:15][CH3:16])[CH:12]=[CH:11][C:7]=1[C:8]([NH:17][C:18]1[CH:34]=[CH:33][CH:32]=[CH:31][C:19]=1[C:20]([NH:22][C:23]1[CH:24]=[CH:25][C:26]([O:29][CH3:30])=[CH:27][CH:28]=1)=[O:21])=[O:10])[CH2:2][CH2:3][CH3:4]참가 물질
3
실험 절차
Using the procedure described in Example 102, Part A, 2-butoxy-4-methoxybenzoic acid (0.54 mmol) and 2-amino-N-(4-methoxyphenyl)benzamide (0.54 mmol) yielded 61 mg (25%) of the title compound.
출처 및 근거
- ORD 기록
- ord-72fe10891037467b885298298edf2ba6
- 출처 데이터셋
- uspto-grants-2003_08
- 특허 번호
- US06605626B2
연결된 노트
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