HCID 22668508, compound → HCID 178486548, compound
Reaction equation
C([N:4]1[C:12]2[C:7](=[CH:8][C:9]([O:15][CH3:16])=[C:10]([O:13][CH3:14])[CH:11]=2)[C:6](=[C:17](OCC)[C:18]2[CH:23]=[CH:22][CH:21]=[CH:20][CH:19]=2)[C:5]1=[O:27])(=O)C.[CH3:28][N:29]([CH3:48])[CH2:30][CH2:31][NH:32][C:33]([CH2:35][N:36]([S:44]([CH3:47])(=[O:46])=[O:45])[C:37]1[CH:42]=[CH:41][C:40]([NH2:43])=[CH:39][CH:38]=1)=[O:34]>>[CH3:28][N:29]([CH3:48])[CH2:30][CH2:31][NH:32][C:33]([CH2:35][N:36]([C:37]1[CH:42]=[CH:41][C:40]([NH:43]/[C:17](=[C:6]2\[C:5](=[O:27])[NH:4][C:12]3[C:7]\2=[CH:8][C:9]([O:15][CH3:16])=[C:10]([O:13][CH3:14])[CH:11]=3)/[C:18]2[CH:23]=[CH:22][CH:21]=[CH:20][CH:19]=2)=[CH:39][CH:38]=1)[S:44]([CH3:47])(=[O:46])=[O:45])=[O:34]Participants
3
Procedure
Prepared from 1-acetyl-3-(1-ethoxy-1-phenyl-methylidene)-5,6-dimethoxy-2-indolinone and N-[(2-dimethylamino-ethylamino)-carbonylmethyl]-N-methylsulphonyl-p-phenylenediamine
Sources & evidence
- ORD record
- ord-be9aec2fb26d4ddcae658685bcb8d6aa
- Source dataset
- uspto-grants-2004_09
- Patent number
- US06794395B1
Reaction notes
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