2,6-Difluoro-3-methoxybenzeneboronic acid → [4-(2,6-Difluoro-3-methoxy-phenyl)-pyridin-3-yl]-methyl-amine
反応式
COC1N=C([C:9]2[CH:14]=[CH:13][N:12]=[CH:11][C:10]=2[N:15](C)[C:16](=O)C2C=C(C(F)(F)F)C=C(C(F)(F)F)C=2)C=CC=1.[F:33][C:34]1[C:39]([O:40][CH3:41])=[CH:38][CH:37]=[C:36]([F:42])[C:35]=1B(O)O>CCCCCC.CCOC(C)=O>[F:33][C:34]1[C:39]([O:40][CH3:41])=[CH:38][CH:37]=[C:36]([F:42])[C:35]=1[C:9]1[CH:14]=[CH:13][N:12]=[CH:11][C:10]=1[NH:15][CH3:16]参加物
4
実験手順
The title compound was prepared in analogy to compound 284, intermediate, from (4-iodo-pyridin-3-yl)-methyl-amine (example 98, intermediate) and 2,6-difluoro-3-methoxyphenylboronic acid and using a gradient of n-hexane:EtOAc (70:30 to 60:40) for the chromatographic purification. Brown solid (75%). MS (ESI): m/z=251.2 [M+H]+.
後処理
- customfor the chromatographic purification
出典と根拠
- ORDレコード
- ord-4f5d57f48af24ae18c882602ee18fb9d
- 出典データセット
- uspto-grants-2015_03
- 特許番号
- US08987307B2
反応ノート
読み込み中…