반응식
[Cl:1][C:2]1[CH:10]=[C:9]([O:11][CH3:12])[CH:8]=[CH:7][C:3]=1[C:4]([OH:6])=[O:5].[F:13][C:14]([F:21])([F:20])[C:15]([NH:17][CH2:18]O)=[O:16].OS(O)(=O)=O>>[F:13][C:14]([F:21])([F:20])[C:15]([NH:17][CH2:18][C:8]1[C:9]([O:11][CH3:12])=[CH:10][C:2]([Cl:1])=[C:3]([CH:7]=1)[C:4]([OH:6])=[O:5])=[O:16]참가 물질
4
실험 절차
The title compound was prepared according to the procedure described in step-1 of Intermediate-26 by using 2-chloro-4-methoxybenzoic acid (0.060 g), 2,2,2-trifluoro-N-(hydroxymethyl)acetamide (0.050 g) and H2SO4 (2 mL) to afford 0.040 g of the desired product.
후처리
- customThe title compound was prepared
출처 및 근거
- ORD 기록
- ord-28def1e1d84f42db8ac98d0a93fae888
- 출처 데이터셋
- uspto-grants-2016_09
- 특허 번호
- US09439890B2
연결된 노트
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