HCID 85869229, compound → HCID 178433425, compound
Reaction equation
[C:1]([NH:4][C:5]1[C:6]([C:13]([NH2:15])=[O:14])=[N:7][NH:8][C:9]=1[CH:10]([CH3:12])[CH3:11])(=O)[CH3:2]>[OH-].[Na+]>[CH3:2][C:1]1[N:15]=[C:13]([OH:14])[C:6]2[NH:7][N:8]=[C:9]([CH:10]([CH3:12])[CH3:11])[C:5]=2[N:4]=1Participants
3
Reactant 1
Product 1
Reagents, catalysts & solvents 1
Procedure
The solution of 4-acetamido-5-isopropylpyrazol-3-carboxamide XX (100 mg, 0.40 mmol) in 1 mL of 1 M sodium hydroxide was stirred at 80-90° C. for 3 hours. The product precipitated after cooling and acidifying with glacial acetic acid. Yield 98%; mp>250° C.; MS (ES+): 193.1 (100%, M+H+). 1H NMR (300 MHz; CD3OD): 1.38 d (6H, J=7.1 Hz); 2.41 s (3H); 3.02 sept (1H, J=7.1 Hz).
Workup
- customThe product precipitated
- temperatureafter cooling
Sources & evidence
- ORD record
- ord-20c7354559d14498ad029ed8370cce2b
- Source dataset
- uspto-grants-2010_06
- Patent number
- US07745450B2
Reaction notes
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