6-hydrazino-1-isobutyl-3-methyl-2,4(1H,3H)-pyrimidinedione → HCID 58981070、化合物
反応式
[NH:1]([C:3]1[N:8]([CH2:9][CH:10]([CH3:12])[CH3:11])[C:7](=[O:13])[N:6]([CH3:14])[C:5](=[O:15])[CH:4]=1)[NH2:2].[F:16][C:17]1[CH:18]=[C:19]2[C:24](=[CH:25][CH:26]=1)[N:23]=[CH:22][CH:21]=[C:20]2[CH:27]=O.[CH3:29][N:30]1[CH:34]=[C:33]([C:35](=[O:38])[CH2:36][CH3:37])[CH:32]=[C:31]1[CH:39]=O>>[F:16][C:17]1[CH:18]=[C:19]2[C:24](=[CH:25][CH:26]=1)[N:23]=[CH:22][CH:21]=[C:20]2[CH2:27][N:2]1[C:39]([C:31]2[N:30]([CH3:29])[CH:34]=[C:33]([C:35](=[O:38])[CH2:36][CH3:37])[CH:32]=2)=[C:4]2[C:3]([N:8]([CH2:9][CH:10]([CH3:11])[CH3:12])[C:7](=[O:13])[N:6]([CH3:14])[C:5]2=[O:15])=[N:1]1参加物
4
実験手順
This compound was made following the procedure described above, starting with 6-hydrazino-1-isobutyl-3-methylpyrimidine-2,4(1H,3H)-dione, and condensing first with 6-fluoroquinoline-4-carbaldehyde, followed by 1-methyl-4-propionyl-1H-pyrrole-2-carbaldehyde. 517 (M+H).
出典と根拠
- ORDレコード
- ord-8c4f2eeb35d94538afa32da0f1683372
- 出典データセット
- uspto-grants-2007_10