HCID 58000837, compound → HCID 178515781, compound
Reaction equation
[Br:1][C:2]1[CH:7]=[CH:6][C:5]([C:8]2[N:9]=[C:10]([C:21]3[CH:26]=[CH:25][CH:24]=[CH:23][C:22]=3[Cl:27])[N:11](O)[C:12]=2[C:13]2[CH:18]=[CH:17][NH:16][C:15](=[O:19])[CH:14]=2)=[CH:4][CH:3]=1>CO>[Br:1][C:2]1[CH:7]=[CH:6][C:5]([C:8]2[N:9]=[C:10]([C:21]3[CH:26]=[CH:25][CH:24]=[CH:23][C:22]=3[Cl:27])[NH:11][C:12]=2[C:13]2[CH:18]=[CH:17][NH:16][C:15](=[O:19])[CH:14]=2)=[CH:4][CH:3]=1Participants
3
Reactant 1
Product 1
Reagents, catalysts & solvents 1
Procedure
Using the general procedure in Example 1 Step D, the intermediate of Example 3 Step A was treated with TiCl3 in methanol. 1H NMR (400 MHz, DMSO-d6): [M+1]+ 427.
Sources & evidence
- ORD record
- ord-21aae8f2321546fdbfcd6664ff4b7deb
- Source dataset
- uspto-grants-2010_07
- Patent number
- US07763634B2
Reaction notes
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