HCID 10516606, compound → HCID 89699802, compound
Reaction equation
[CH2:1]([O:3][CH:4]([O:18][CH2:19][CH3:20])[CH2:5][N:6]1[C:10]([NH2:11])=[CH:9][C:8]([C:12]2[CH:13]=[N:14][CH:15]=[CH:16][CH:17]=2)=[N:7]1)[CH3:2].Br[C:22]1[CH:27]=[CH:26][CH:25]=[C:24]([N+:28]([O-:30])=[O:29])[C:23]=1[F:31]>>[CH2:1]([O:3][CH:4]([O:18][CH2:19][CH3:20])[CH2:5][N:6]1[C:10]([NH:11][C:22]2[CH:27]=[CH:26][CH:25]=[C:24]([N+:28]([O-:30])=[O:29])[C:23]=2[F:31])=[CH:9][C:8]([C:12]2[CH:13]=[N:14][CH:15]=[CH:16][CH:17]=2)=[N:7]1)[CH3:2]Participants
3
Procedure
Analogously to the process described in Example 64A/Step 1, 1.0 g (3.62 mmol) of the compound of Example 4A and 876 mg (3.98 mmol) of 1-bromo-2-fluoro-3-nitrobenzene gave 1.11 g (73% of theory) of the title compound.
Sources & evidence
- ORD record
- ord-1a70341973fb458796f37d9789a52e74
- Source dataset
- uspto-grants-2016_07
- Patent number
- US09394309B2
Reaction notes
Loading…