Water → HCID 178517247, compound
Reaction equation
C([N:4]1[C:12]2[C:7](=[CH:8][C:9]([N+:13]([O-:15])=[O:14])=[CH:10][CH:11]=2)[C:6](=[C:16](OCC)[C:17]2[CH:22]=[CH:21][CH:20]=[CH:19][CH:18]=2)[C:5]1=[O:26])(=O)C.[NH2:27][C:28]1[CH:33]=[CH:32][C:31]([C:34]2[NH:38][N:37]=[N:36][N:35]=2)=[CH:30][CH:29]=1.N1CCCCC1.O>CN(C=O)C>[NH:38]1[C:34]([C:31]2[CH:32]=[CH:33][C:28]([NH:27]/[C:16](=[C:6]3\[C:5](=[O:26])[NH:4][C:12]4[C:7]\3=[CH:8][C:9]([N+:13]([O-:15])=[O:14])=[CH:10][CH:11]=4)/[C:17]3[CH:22]=[CH:21][CH:20]=[CH:19][CH:18]=3)=[CH:29][CH:30]=2)=[N:35][N:36]=[N:37]1Participants
6
Procedure
Prepared by reacting 1-acetyl-3-{1-ethoxy-1-phenylmethylidene}-5-nitro-2-indolinone with 1.3 equivalents of 5-(4-amino-phenyl)-1H-tetrazole in DMF (125° C., for 2 hours), subsequent treatment with 6.7 equivalents of piperidine (20° C., 1 hour) and precipitation with water.
Workup
- customPrepared
Sources & evidence
- ORD record
- ord-00f7ca05e96942e3bf4188d52f893741
- Source dataset
- uspto-grants-2000_03
- Patent number
- US06043254
Reaction notes
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