Sodium Hydroxide → HCID 59579953, compound
Reaction equation
[NH2:1][C:2]1[C:7]([F:8])=[CH:6][N:5]=[C:4]([N:9]2[CH:13]=[C:12]([C:14]([O:16]CC)=[O:15])[C:11]([C:19]([F:22])([F:21])[F:20])=[N:10]2)[N:3]=1.[OH-].[Na+]>CO>[NH2:1][C:2]1[C:7]([F:8])=[CH:6][N:5]=[C:4]([N:9]2[CH:13]=[C:12]([C:14]([OH:16])=[O:15])[C:11]([C:19]([F:22])([F:21])[F:20])=[N:10]2)[N:3]=1Participants
4
Reactant 2
Product 1
Reagents, catalysts & solvents 1
Procedure
A solution of ethyl 1-(4-amino-5-fluoropyrimidin-2-yl)-3-(trifluoromethyl)-1H-pyrazole-4-carboxylate (269 mg, 0.84 mmol) and NaOH (2 mL, 10N) in MeOH is heated to 45° C. for 2 h. The solvent is removed to dryness. H2O is added. The solution is acidified with 2N HCl to pH=5, to afford the title compound as an off-white solid.
Workup
- customThe solvent is removed to dryness
- additionH2O is added
Sources & evidence
- ORD record
- ord-f0686ddea44e48d1a30be91e7afd0072
- Source dataset
- uspto-grants-2015_09
- Patent number
- US09133204B2
Reaction notes
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