2-Amino-4,6-difluoropyrimidine → 4,6-difluoro-N-((2-phenylimidazo[1,2-a]pyridin-3-yl)methyl)pyrimidin-2-amine
反応式
Cl.Cl[CH2:3][C:4]1[N:8]2[CH:9]=[CH:10][CH:11]=[CH:12][C:7]2=[N:6][C:5]=1[C:13]1[CH:18]=[CH:17][CH:16]=[CH:15][CH:14]=1.[F:19][C:20]1[CH:25]=[C:24]([F:26])[N:23]=[C:22]([NH2:27])[N:21]=1>>[F:19][C:20]1[CH:25]=[C:24]([F:26])[N:23]=[C:22]([NH:27][CH2:3][C:4]2[N:8]3[CH:9]=[CH:10][CH:11]=[CH:12][C:7]3=[N:6][C:5]=2[C:13]2[CH:18]=[CH:17][CH:16]=[CH:15][CH:14]=2)[N:21]=1参加物
3
実験手順
The title compound was prepared according to Method A and the experimentals described for compound 139 from 3-(chloromethyl)-2-phenylimidazo[1,2-a]pyridine hydrochloride and 4,6-difluoropyrimidin-2-amine. (0.10 g, 17% yield), M/e− 338.2 for C18H13F2N5 (M+H)+
出典と根拠
- ORDレコード
- ord-16f9e0327caf4022bd770cac06923ce3
- 出典データセット
- uspto-grants-2013_07
- 特許番号
- US08497278B2
反応ノート
読み込み中…