HCID 18466607, compound → HCID 18466603, compound
Reaction equation
[CH2:1]([NH:3][C:4]1[C:9]([N+:10]([O-])=O)=[CH:8][CH:7]=[C:6]([C:13]([F:16])([F:15])[F:14])[N:5]=1)[CH3:2]>CO.[OH-].[OH-].[Pd+2]>[NH2:10][C:9]1[C:4]([NH:3][CH2:1][CH3:2])=[N:5][C:6]([C:13]([F:14])([F:15])[F:16])=[CH:7][CH:8]=1Participants
4
Reactant 1
Product 1
Reagents, catalysts & solvents 2
Procedure
A solution of 2-(ethylamino)-3-nitro-6-(trifluoromethyl)pyridine (1.1 g, 4.9 mmol) in MeOH (40 mL) was stirred overnight at room temperature under hydrogen (1 atm.) in the presence of 20% Pd(OH)2/C (100 mg). The catalyst was removed by filtration through diatomaceous earth. The filtrate was concentrated under reduced pressure to give the title compound as an orange oil (1 g).
Workup
- customThe catalyst was removed by filtration through diatomaceous earth
- concentrationThe filtrate was concentrated under reduced pressure
Sources & evidence
- ORD record
- ord-d342be6adbd74fe3bcec0faf7549de82
- Source dataset
- uspto-grants-2002_07
- Patent number
- US06420359B1
Reaction notes
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