P-Anisidine → 3-(4-Methoxybenzoyl)amino-N-(4-methoxyphenyl)-2-indolecarboxamide
반응식
[CH3:1][O:2][C:3]1[CH:8]=[CH:7][C:6]([NH2:9])=[CH:5][CH:4]=1.[CH3:10][O:11][C:12]1[CH:32]=[CH:31][C:15]([C:16]([NH:18][C:19]2[C:27]3[C:22](=[CH:23][CH:24]=[CH:25][CH:26]=3)[NH:21][C:20]=2[C:28](O)=[O:29])=[O:17])=[CH:14][CH:13]=1.Cl.CN(C)CCCN=C=NCC>C(Cl)Cl.CN(C)C1C=CN=CC=1>[CH3:10][O:11][C:12]1[CH:13]=[CH:14][C:15]([C:16]([NH:18][C:19]2[C:27]3[C:22](=[CH:23][CH:24]=[CH:25][CH:26]=3)[NH:21][C:20]=2[C:28]([NH:9][C:6]2[CH:7]=[CH:8][C:3]([O:2][CH3:1])=[CH:4][CH:5]=2)=[O:29])=[O:17])=[CH:31][CH:32]=1참가 물질
6
반응물 3
생성물 1
시약·촉매·용매 2
실험 절차
To a solution p-anisidine (79 mg, 0.645 mmol) in methylene chloride (5 mL) was added 3-(4-methoxybenzoyl)amino-2-indolecarboxylic acid (200 mg, 0.645 mmol), 1-(3-dimethylaminopropyl)-3-ethylcarbodiimide hydrochloride (247 mg, 1.29 mmol), and 4-dimethylaminopyridine (8.0 mg, 0.065 mmol). The resulting solution was stirred at room temperature for 6 h. The resulting precipitate was collected via vacuum filtration to provide 38 mg (14%) of the title compound as a white solid.
후처리
- filtrationThe resulting precipitate was collected via vacuum filtration
출처 및 근거
- ORD 기록
- ord-ea68df5daac349e185019f1ba29715da
- 출처 데이터셋
- uspto-grants-2003_07
- 특허 번호
- US06586459B2
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