2-Amino-4-(trifluoromethyl)pyridine → HCID 86660386, compound
Reaction equation
[N+:1]([C:4]1[CH:5]=[C:6]([CH:10]=[CH:11][C:12]=1[N+:13]([O-:15])=[O:14])[C:7](Cl)=[O:8])([O-:3])=[O:2].[NH2:16][C:17]1[CH:22]=[C:21]([C:23]([F:26])([F:25])[F:24])[CH:20]=[CH:19][N:18]=1>>[N+:1]([C:4]1[CH:5]=[C:6]([CH:10]=[CH:11][C:12]=1[N+:13]([O-:15])=[O:14])[C:7]([NH:16][C:17]1[CH:22]=[C:21]([C:23]([F:25])([F:24])[F:26])[CH:20]=[CH:19][N:18]=1)=[O:8])([O-:3])=[O:2]Participants
3
Procedure
Prepared analogously to example 303a from 3,4-dinitro-benzoyl chloride and 2-amino-4-trifluoromethyl-pyridine.
Sources & evidence
- ORD record
- ord-327ac822e38b4ecaad72bcf9a3359a0a
- Source dataset
- uspto-grants-2014_12
- Patent number
- US08916599B2
Reaction notes
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