反応式
[C:1]1([C:7]2[N:12]=[C:11]([OH:13])[C:10]3[CH2:14][CH2:15][CH2:16][C:9]=3[N:8]=2)[CH:6]=[CH:5][CH:4]=[CH:3][CH:2]=1.[F:17][C:18]1[CH:25]=[CH:24][C:21]([CH2:22]Br)=[CH:20][CH:19]=1>>[F:17][C:18]1[CH:25]=[CH:24][C:21]([CH2:22][O:13][C:11]2[C:10]3[CH2:14][CH2:15][CH2:16][C:9]=3[N:8]=[C:7]([C:1]3[CH:2]=[CH:3][CH:4]=[CH:5][CH:6]=3)[N:12]=2)=[CH:20][CH:19]=1参加物
3
実験手順
The title compound was prepared from 2-phenyl-6,7-dihydro-5H-cyclopentapyrimidin-4-ol (which was obtained in Intermediate 5) and 4-fluorobenzyl bromide according to Method A; LC retention time 3.26 min; MS: m/z (ESI) 321 (M+H).
出典と根拠
- ORDレコード
- ord-427b996b8384497b91c8121c533f3034
- 出典データセット
- uspto-grants-2008_09
- 特許番号
- US07423044B2
関連ノート
読み込み中…