HCID 21139221, compound → HCID 59077645, compound
Reaction equation
[C:1]1([CH2:7][S:8]([C:11]2[CH:12]=[C:13]3[C:17](=[CH:18][CH:19]=2)[NH:16][C:15](=[O:20])[CH2:14]3)(=[O:10])=[O:9])[CH:6]=[CH:5][CH:4]=[CH:3][CH:2]=1.[CH:21]([C:23]1[NH:27][C:26]([CH3:28])=[C:25]([CH2:29][C:30]([OH:32])=[O:31])[C:24]=1[CH3:33])=O>>[CH3:28][C:26]1[NH:27][C:23](/[CH:21]=[C:14]2\[C:15](=[O:20])[NH:16][C:17]3[C:13]\2=[CH:12][C:11]([S:8]([CH2:7][C:1]2[CH:2]=[CH:3][CH:4]=[CH:5][CH:6]=2)(=[O:10])=[O:9])=[CH:19][CH:18]=3)=[C:24]([CH3:33])[C:25]=1[CH2:29][C:30]([OH:32])=[O:31]Participants
3
Procedure
5-Phenylmethanesulfonyl-1,3-dihydro-indol-2-one was condensed with (5-formyl-2,4-dimethyl-1H-pyrrol-3-yl)-acetic acid to give the titled compound.
Sources & evidence
- ORD record
- ord-cde1785994104798a41adfb1647021d0
- Source dataset
- uspto-grants-2003_07
- Patent number
- US06599902B2
Reaction notes
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