Nitric Acid → HCID 178496181, compound
Reaction equation
[Cl:1][C:2]1[CH:20]=[CH:19][C:5]([C:6]([NH:8][C@H:9]2[CH2:14][CH2:13][C@H:12]([C:15]([F:18])([F:17])[F:16])[CH2:11][CH2:10]2)=[O:7])=[C:4]([O:21][CH2:22][CH2:23][O:24][CH3:25])[N:3]=1.[N+:26]([O-])([OH:28])=[O:27]>OS(O)(=O)=O>[Cl:1][C:2]1[C:20]([N+:26]([O-:28])=[O:27])=[CH:19][C:5]([C:6]([NH:8][C@H:9]2[CH2:14][CH2:13][C@H:12]([C:15]([F:18])([F:17])[F:16])[CH2:11][CH2:10]2)=[O:7])=[C:4]([O:21][CH2:22][CH2:23][O:24][CH3:25])[N:3]=1Participants
4
Reactant 2
Product 1
Reagents, catalysts & solvents 1
Procedure
The sub-title compound is prepared from 6-chloro-2-(2-methoxy-ethoxy)-N-(trans-4-trifluoromethyl-cyclohexyl)-nicotinamide (2.20 g, 5.78 mmol), fuming HNO3 (5 mL) and conc. H2SO4 (10 mL) in analogy to example 1c.
Sources & evidence
- ORD record
- ord-3e770a5852c2492994eea3b4e9770be0
- Source dataset
- uspto-grants-2013_11
- Patent number
- US08586604B2
Reaction notes
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