반응식
F[C:2]1[C:7](F)=[CH:6][C:5]([C:9]2[CH:14]=[CH:13][N:12]=[CH:11][C:10]=2[N:15]([CH2:32]CS(C)(=O)=O)C(=O)C2C=C(C(F)(F)F)N=C(C(F)(F)F)C=2)=[C:4]([O:38][CH3:39])[CH:3]=1.[CH3:40][O:41]C1C(OC)=CC=CC=1B(O)O>CCCCCCC.CCOC(C)=O>[CH3:39][O:38][C:4]1[C:3]([O:41][CH3:40])=[CH:2][CH:7]=[CH:6][C:5]=1[C:9]1[CH:14]=[CH:13][N:12]=[CH:11][C:10]=1[NH:15][CH3:32]참가 물질
4
실험 절차
The title compound was prepared in analogy to example 72, from (4-iodo-pyridin-3-yl)-methyl-amine (example 98, intermediate b) and 2,3-dimethoxyphenylboronic acid (CAS RN 28611-39-4) and using a gradient of n-heptane:EtOAc (100:0 to 30:70) for the chromatographic purification. Light yellow solid (79%). MS (ESI): m/z=245.128 [M+H]+.
후처리
- customfor the chromatographic purification
출처 및 근거
- ORD 기록
- ord-c369cf86c47b4affa9f9d9bf4de5ead8
- 출처 데이터셋
- uspto-grants-2015_03
- 특허 번호
- US08987307B2
연결된 노트
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