1,8-Diazabicyclo(5.4.0)undec-7-ene → 2-(2-Methyl-imidazol-1-yl)-7-pyridin-2-yl-[1,2,4]triazolo[1,5-a]pyridin-5-ylamine
反応式
CS([C:4]1[N:19]=[C:7]2[CH:8]=[C:9]([C:13]3[CH:18]=[CH:17][CH:16]=[CH:15][N:14]=3)[CH:10]=[C:11]([NH2:12])[N:6]2[N:5]=1)=O.[N:20]12[CH2:30][CH2:29]C[N:27]=[C:26]1[CH2:25]CCCC2>CC1NC=CN=1>[CH3:25][C:26]1[N:20]([C:4]2[N:19]=[C:7]3[CH:8]=[C:9]([C:13]4[CH:18]=[CH:17][CH:16]=[CH:15][N:14]=4)[CH:10]=[C:11]([NH2:12])[N:6]3[N:5]=2)[CH:30]=[CH:29][N:27]=1参加物
4
実験手順
The title compound, MS m/e (%):292 (M+H+,100), was prepared in accordance with the method of example 339b) from 2-methanesulfinyl-7-pyridin-2-yl-[1,2,4]triazolo[1,5-a]pyridin-5-ylamine and 1,8-diazabicyclo[5.4.0]undec-7-en in 2-methylimidazole at 170° C.
出典と根拠
- ORDレコード
- ord-6bfe6746b57c4ed5bae45fa92cce01fc
- 出典データセット
- uspto-grants-2002_03
- 特許番号
- US06355653B1
反応ノート
読み込み中…