N-hydroxysuccinimide-ammonium salt → HCID 178456748, compound
Reaction equation
[C:1]([CH2:4][C:5]1[CH:28]=[CH:27][C:8]([NH:9]/[C:10](=[C:13]2\[C:14](=[O:26])[NH:15][C:16]3[C:21]\2=[CH:20][C:19]([O:22][CH3:23])=[C:18]([O:24][CH3:25])[CH:17]=3)/[CH2:11][CH3:12])=[CH:7][CH:6]=1)([OH:3])=O.[NH4+].O[N:31]1C(=O)CCC1=O>>[NH2:31][C:1]([CH2:4][C:5]1[CH:28]=[CH:27][C:8]([NH:9]/[C:10](=[C:13]2\[C:14](=[O:26])[NH:15][C:16]3[C:21]\2=[CH:20][C:19]([O:22][CH3:23])=[C:18]([O:24][CH3:25])[CH:17]=3)/[CH2:11][CH3:12])=[CH:7][CH:6]=1)=[O:3]Participants
3
Procedure
Prepared from 3-(Z)-{1-[4-(carboxymethyl)-anilino]-1-ethyl-methylidene}-5,6-dimethoxy-2-indolinone and N-hydroxy-succinimide-ammonium salt
Sources & evidence
- ORD record
- ord-a905c010f5384fbb8053832c68ffce6e
- Source dataset
- uspto-grants-2004_09
- Patent number
- US06794395B1
Reaction notes
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