반응식
[F:1][C:2]([F:19])([F:18])[C:3]([NH:5][CH2:6][C:7]1[C:8]([F:17])=[CH:9][C:10]([Cl:16])=[C:11]([CH:15]=1)C(O)=O)=[O:4].OS(O)(=O)=O.[N-:25]=[N+]=[N-].[Na+]>>[NH2:25][C:11]1[C:10]([Cl:16])=[CH:9][C:8]([F:17])=[C:7]([CH:15]=1)[CH2:6][NH:5][C:3](=[O:4])[C:2]([F:19])([F:18])[F:1]참가 물질
4
실험 절차
The title compound was prepared according to the procedure described in step-1 of Intermediate-57 by using 5-((2,2,2-trifluoroacetamido)methyl)-2-chloro-4-fluorobenzoic acid (3.0 g), conc. H2SO4 and sodium azide (0.793 g, 0.012 mmol) to afford 2.1 g of the desired product.
후처리
- customThe title compound was prepared
출처 및 근거
- ORD 기록
- ord-069b0936d7534524b20bdb7e804dfc9b
- 출처 데이터셋
- uspto-grants-2016_09
- 특허 번호
- US09439890B2
연결된 노트
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