(5,6-dihydro-4H-pyrrolo[3,2,1-ij]quinolin-1-yl)acetamide → HCID 22556696, compound
Reaction equation
C[O:2][C:3](=O)[C:4]([C:6]1[C:14]2[C:9](=[C:10]([CH2:15][CH2:16][CH2:17][O:18][Si:19]([CH:26]([CH3:28])[CH3:27])([CH:23]([CH3:25])[CH3:24])[CH:20]([CH3:22])[CH3:21])[CH:11]=[CH:12][CH:13]=2)[NH:8][CH:7]=1)=O.[C:30]1([CH2:42][C:43]([NH2:45])=[O:44])[C:40]2=[C:41]3[C:36](=[CH:37][CH:38]=[CH:39]2)[CH2:35][CH2:34][CH2:33][N:32]3[CH:31]=1>>[C:30]1([C:42]2[C:43](=[O:44])[NH:45][C:3](=[O:2])[C:4]=2[C:6]2[C:14]3[C:9](=[C:10]([CH2:15][CH2:16][CH2:17][O:18][Si:19]([CH:23]([CH3:25])[CH3:24])([CH:26]([CH3:28])[CH3:27])[CH:20]([CH3:22])[CH3:21])[CH:11]=[CH:12][CH:13]=3)[NH:8][CH:7]=2)[C:40]2=[C:41]3[C:36](=[CH:37][CH:38]=[CH:39]2)[CH2:35][CH2:34][CH2:33][N:32]3[CH:31]=1Participants
3
Procedure
Beginning with 7-((triisopropylsilyloxy)propyl)indole-3-glyoxylic acid methyl ester and 2-(5,6-dihydro-4H-pyrrolo[3,2,1-ij]quinolin-1-yl)acetamide, the title compound was prepared essentially as described in Example 1.
Sources & evidence
- ORD record
- ord-7c3acc2076ad402da46d0ba3d0d37e4e
- Source dataset
- uspto-grants-2005_03