4-(Tetramethyl-1,3,2-dioxaborolan-2-yl)aniline → (S)-4-(6-(5-fluoro-2-(methylsulfonyl)phenyl)-2-(3-methylmorpholino)pyrimidin-4-yl)aniline
反応式
F[C:2]1[CH:3]=[C:4]([C:8]2[N:13]=C(SC)N=[C:10](N3CCOC[C@@H]3C)[CH:9]=2)C=NC=1.Cl[C:24]1[CH:29]=[C:28]([C:30]2[CH:35]=[C:34]([F:36])[CH:33]=[CH:32][C:31]=2[S:37]([CH3:40])(=[O:39])=[O:38])[N:27]=[C:26]([N:41]2[CH2:46][CH2:45][O:44][CH2:43][C@@H:42]2[CH3:47])[N:25]=1.CC1(C)C(C)(C)OB(C2C=CC(N)=CC=2)O1>>[F:36][C:34]1[CH:33]=[CH:32][C:31]([S:37]([CH3:40])(=[O:39])=[O:38])=[C:30]([C:28]2[N:27]=[C:26]([N:41]3[CH2:46][CH2:45][O:44][CH2:43][C@@H:42]3[CH3:47])[N:25]=[C:24]([C:2]3[CH:3]=[CH:4][C:8]([NH2:13])=[CH:9][CH:10]=3)[CH:29]=2)[CH:35]=1参加物
4
反応物 3
生成物 1
実験手順
Method as described for intermediate 5 using (S)-4-(4-chloro-6-(5-fluoro-2-(methylsulfonyl)phenyl)pyrimidin-2-yl)-3-methylmorpholine (intermediate 16) (451 mg, 1.17 mmol) and 4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)aniline (256 mg, 1.17 mmol). The mixture was purified using flash chromatography (30-100% EtOAc in petroleum ether 40-60) to afford the title compound (298 mg, 58%)
後処理
- customThe mixture was purified
出典と根拠
- ORDレコード
- ord-2bf03ae669c545088fc452884e520f1f
- 出典データセット
- uspto-grants-2016_02
- 特許番号
- US09249129B2
反応ノート
読み込み中…