HCID 21999021, compound → HCID 21999037, compound
Reaction equation
[N:1]([C:4]1[CH:12]=[C:11]2[C:7]([C:8]([C:14](=O)[C:15](Cl)=[O:16])=[CH:9][N:10]2[CH3:13])=[CH:6][CH:5]=1)=[N+:2]=[N-:3].Cl.C([O:23][C:24](=[NH:38])[CH2:25][C:26]1[C:34]2[C:29](=[CH:30][C:31]([O:35][CH3:36])=[CH:32][CH:33]=2)[N:28]([CH3:37])[CH:27]=1)(C)C>>[N:1]([C:4]1[CH:12]=[C:11]2[C:7]([C:8]([C:14]3[C:15](=[O:16])[NH:38][C:24](=[O:23])[C:25]=3[C:26]3[C:34]4[C:29](=[CH:30][C:31]([O:35][CH3:36])=[CH:32][CH:33]=4)[N:28]([CH3:37])[CH:27]=3)=[CH:9][N:10]2[CH3:13])=[CH:6][CH:5]=1)=[N+:2]=[N-:3]Participants
3
Procedure
3-(6-Azido-1-methyl-1H-indol-3-yl)-4-(6-methoxy-1-methyl-1H-indol-3-yl)-pyrrole-2,5,-dione was prepared from (6-azido-1-methyl-1H-indol-3-yl)-oxo-acetyl chloride and 2-(6-methoxy-1-methyl-1H-indol-3-yl)-acetimidic acid isopropyl ester hydrochloride.
Sources & evidence
- ORD record
- ord-b25a0061d7754491a61c5cd8bb6337a8
- Source dataset
- uspto-grants-2001_05
- Patent number
- US06228877B1
Reaction notes
Loading…