Reaction equation
[Br:1][C:2]1[CH:3]=[C:4]2[C:8](=[CH:9][CH:10]=1)[N:7]([C:11]1[CH:19]=[CH:18][CH:17]=[CH:16][C:12]=1[C:13]([NH2:15])=[O:14])[CH2:6][CH2:5]2.BrC1C=C2C(=C([N+:30]([O-:32])=[O:31])C=1)N(C1(C=CC=CC1)C(N)=O)CC2>>[Br:1][C:2]1[CH:3]=[C:4]2[C:8](=[C:9]([N+:30]([O-:32])=[O:31])[CH:10]=1)[N:7]([C:11]1[CH:19]=[CH:18][CH:17]=[CH:16][C:12]=1[C:13]([NH2:15])=[O:14])[CH2:6][CH2:5]2Participants
3
Procedure
It is predicted that if the 2-(5-bromo-indolin-1-yl)benzamide of Example 13a is treated in the manner of Example 1b that 1-(5-bromo-7-nitro-1-indolinyl)benzamide will be obtained.
Workup
- customwill be obtained
Sources & evidence
- ORD record
- ord-775c015a46eb479d8e3c78b8742e1dc4
- Source dataset
- uspto-grants-1988_08
- Patent number
- US04764616
Linked notes
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