HCID 10516606, compound → 1-(2,2-Diethoxyethyl)-N-[5-nitro-2-(trifluoromethyl)phenyl]-3-(pyridin-3-yl)-1H-pyrazole-5-amine
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]=[C:26]([N+:28]([O-:30])=[O:29])[CH:25]=[CH:24][C:23]=1[C:31]([F:34])([F:33])[F:32]>>[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]=[C:26]([N+:28]([O-:30])=[O:29])[CH:25]=[CH:24][C:23]=2[C:31]([F:32])([F:34])[F:33])=[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 Example 13A/Step 1, 1.50 g (5.43 mmol) of the compound of Example 4A and 1.47 g (5.43 mmol) of 2-bromo-4-nitro-1-(trifluoromethyl)benzene gave 2.03 g (75% of theory) of the title compound.
Sources & evidence
- ORD record
- ord-817aea69d02e4bd1afeaa823e8b65f1c
- Source dataset
- uspto-grants-2016_07
- Patent number
- US09394309B2
Reaction notes
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