반응식
[F:1][C:2]1[CH:3]=[C:4]([CH:8]=[CH:9][C:10]=1[C:11]([F:14])([F:13])[F:12])[C:5]([NH2:7])=[O:6].C(Cl)(=O)[C:16](Cl)=[O:17]>C(Cl)CCl>[F:1][C:2]1[CH:3]=[C:4]([CH:8]=[CH:9][C:10]=1[C:11]([F:12])([F:13])[F:14])[C:5]([N:7]=[C:16]=[O:17])=[O:6]참가 물질
4
실험 절차
The title compound was prepared according to the procedure described in step-2 of Intermediate-8 by using 3-fluoro-4-(trifluoromethyl)benzamide (0.200 g), oxalyl chloride (0.025 mL) and EDC (15 mL) to afford 0.150 g of the desired product.
후처리
- customThe title compound was prepared
출처 및 근거
- ORD 기록
- ord-74361060740d4bcb80adf5f17efd1456
- 출처 데이터셋
- uspto-grants-2015_08
- 특허 번호
- US09096545B2
연결된 노트
불러오는 중…