2-(4-fluoro-1H-indol-3-yl)acetamide → 3-(4-Methyl-5,6-dihydro-4H-pyrrolo[3,2,1-ij]quinolin-1-yl)-4-(4-fluoro-1H-indol-3-yl)pyrrole-2,5-dione
反応式
[F:1][C:2]1[CH:10]=[CH:9][CH:8]=[C:7]2[C:3]=1[C:4]([CH2:11][C:12]([NH2:14])=[O:13])=[CH:5][NH:6]2.C[O:16][C:17](=O)[C:18]([C:20]1[C:30]2=[C:31]3[C:26](=[CH:27][CH:28]=[CH:29]2)[CH2:25][CH2:24][CH:23]([CH3:32])[N:22]3[CH:21]=1)=O>>[CH3:32][CH:23]1[CH2:24][CH2:25][C:26]2[C:31]3=[C:30]([C:20]([C:18]4[C:17](=[O:16])[NH:14][C:12](=[O:13])[C:11]=4[C:4]4[C:3]5[C:7](=[CH:8][CH:9]=[CH:10][C:2]=5[F:1])[NH:6][CH:5]=4)=[CH:21][N:22]13)[CH:29]=[CH:28][CH:27]=2参加物
3
実験手順
Beginning with (4-fluoroindol-3-yl)acetamide and (4-methyl-5,6-dihydro-4H-pyrrolo[3,2,1-ij]quinolin-1-yl)oxo-acetic acid methyl ester, the title compound was prepared essentially as described in Example 1.
出典と根拠
- ORDレコード
- ord-50cfbf554fa64364be364f0f377e5327
- 出典データセット
- uspto-grants-2005_03
- DOI