HCID 23507609, compound → HCID 178498056, compound
Reaction equation
[CH3:1][O:2][C:3]([CH:5]1[CH2:9][CH2:8][CH2:7][N:6]1[CH2:10][C:11]1[CH:17]=[CH:16][C:14]([NH2:15])=[CH:13][CH:12]=1)=[O:4].C(O[C:21](=[C:28]1[C:36]2[C:31](=[CH:32][CH:33]=[C:34]([N+:37]([O-:39])=[O:38])[CH:35]=2)[NH:30][C:29]1=[O:40])[C:22]1[CH:27]=[CH:26][CH:25]=[CH:24][CH:23]=1)C>CN(C=O)C>[CH3:1][O:2][C:3]([CH:5]1[CH2:9][CH2:8][CH2:7][N:6]1[CH2:10][C:11]1[CH:12]=[CH:13][C:14]([NH:15]/[C:21](=[C:28]2\[C:29](=[O:40])[NH:30][C:31]3[C:36]\2=[CH:35][C:34]([N+:37]([O-:39])=[O:38])=[CH:33][CH:32]=3)/[C:22]2[CH:23]=[CH:24][CH:25]=[CH:26][CH:27]=2)=[CH:16][CH:17]=1)=[O:4]Participants
4
Reactant 2
Product 1
Reagents, catalysts & solvents 1
Procedure
Prepared from 4-(2-methoxycarbonyl-pyrrolidin-1-ylmethyl)-aniline and 3-(1-ethoxy-1-phenylmethylidene)-5-nitro-2-indolinone in DMF.
Sources & evidence
- ORD record
- ord-085b2490f3f84777b93f5865a167727d
- Source dataset
- uspto-grants-2000_03
- Patent number
- US06043254
Reaction notes
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