Sodium Hydroxide → HCID 86669311, compound
Reaction equation
C[O:2][C:3](=[O:19])[C:4]1[CH:9]=[C:8]([N+:10]([O-:12])=[O:11])[C:7]([NH2:13])=[N:6][C:5]=1[O:14][CH2:15][CH:16]([F:18])[F:17].[OH-].[Na+]>>[F:18][CH:16]([F:17])[CH2:15][O:14][C:5]1[N:6]=[C:7]([NH2:13])[C:8]([N+:10]([O-:12])=[O:11])=[CH:9][C:4]=1[C:3]([OH:19])=[O:2]Participants
3
Procedure
The sub-title compound is prepared from 2-(2,2-difluoro-ethoxy)-6-amino-5-nitro-nicotinic acid methyl ester (1.3 g, 4.8 mmol) and 1 M NaOH in analogy to example 1e. Yield: 0.88 g (70%).
Sources & evidence
- ORD record
- ord-f38fd1f37b6542c2905509f6f3179e53
- Source dataset
- uspto-grants-2013_11
- Patent number
- US08586604B2
Reaction notes
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