反応式
C([O:3][C:4]([C:6]1[CH:7]=[N:8][N:9]([CH3:26])[C:10]=1[C:11](=[O:25])[NH:12][C:13]1[CH:14]=[CH:15][C:16]2[N:17]([N:19]=[C:20]([N:22]([CH3:24])[CH3:23])[N:21]=2)[CH:18]=1)=[O:5])C.CN1C(C(=O)NC2C=CC3N(N=C(N4CCOCC4)N=3)C=2)=C(C(O)=O)C=N1>>[CH3:23][N:22]([CH3:24])[C:20]1[N:21]=[C:16]2[CH:15]=[CH:14][C:13]([NH:12][C:11]([C:10]3[N:9]([CH3:26])[N:8]=[CH:7][C:6]=3[C:4]([OH:5])=[O:3])=[O:25])=[CH:18][N:17]2[N:19]=1参加物
3
反応物 2
生成物 1
実験手順
Using 5-(2-dimethylamino-[1,2,4]triazolo[1,5-a]pyridin-6-ylcarbamoyl)-1-methyl-1H-pyrazole-4-carboxylic acid ethyl ester, this compound was prepared following the same method as for the synthesis of 1-Methyl-5-(2-morpholino-[1,2,4]triazolo[1,5-a]pyridin-6-ylcarbamoyl)-1H-pyrazole-4-carboxylic acid. Brown solid (41 mg, 70%). MS: m/z=330 (M+H+).
後処理
- customthis compound was prepared
出典と根拠
- ORDレコード
- ord-b4dd510c39a54a739c58318f0694d6dc
- 出典データセット
- uspto-grants-2015_02
- 特許番号
- US08946427B2
関連ノート
読み込み中…