반응식
[C:1]([NH:4][C:5]1[CH:6]=[CH:7][C:8](Br)=[C:9]([CH:13]=1)[C:10]([OH:12])=[O:11])(=[O:3])[CH3:2].CN(C=O)C.[NH2:20][C:21]1[N:25]([CH2:26][CH3:27])[N:24]=[CH:23][CH:22]=1.C([O-])([O-])=O.[K+].[K+]>CC([O-])=O.CC([O-])=O.[Cu+2].C(O)(=O)C.O>[CH2:26]([N:25]1[C:21]([NH:20][C:8]2[C:9](=[CH:13][C:5]([NH:4][C:1](=[O:3])[CH3:2])=[CH:6][CH:7]=2)[C:10]([OH:12])=[O:11])=[CH:22][CH:23]=[N:24]1)[CH3:27]참가 물질
8
실험 절차
A mixture of 5-acetamido-2-bromobenzoic acid (7 g, 27 mmol), DMF (25 ml), Cu(OAc)2 (0.2 g), 5-amino-1-ethyl-pyrazole (3 g, 27 mmol) and K2CO3 (3.7 g, 27 mmol) was refluxed for about 2 days. The reaction mixture was poured into water, acidified with acetic acid and cooled. A solid formed which was collected by filtration to afford 2 g of N-(1-ethylpyrazole-5-yl)-5-acetamidoanthranilic acid.
후처리
- temperaturewas refluxed for about 2 days
- temperaturecooled
- customA solid formed which
- filtrationwas collected by filtration
출처 및 근거
- ORD 기록
- ord-cdc0a5941aae4020a43435d52afd34bb
- 출처 데이터셋
- uspto-grants-1996_01
- 특허 번호
- US05488055
연결된 노트
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