Hydrochloric Acid → HCID 68641848, compound
Reaction equation
[OH-].[Na+].[Cl:3][C:4]1[CH:9]=[CH:8][C:7]([C:10]2[CH:11]=[C:12]([C:15]([O:17]C)=[O:16])[NH:13][N:14]=2)=[C:6]([O:19][CH3:20])[CH:5]=1.Cl>C(O)C>[Cl:3][C:4]1[CH:9]=[CH:8][C:7]([C:10]2[CH:11]=[C:12]([C:15]([OH:17])=[O:16])[NH:13][N:14]=2)=[C:6]([O:19][CH3:20])[CH:5]=1Participants
5
Reactant 3
Product 1
Reagents, catalysts & solvents 1
Procedure
Ethanol (1 ml) and a 20% sodium hydroxide aqueous solution were mixed with methyl 5-(4-chloro-2-methoxyphenyl)-2H-pyrazole-3-carboxylate (100 mg) obtained in the Step 18-1-2, and the mixture was heated under reflux. After one hour, the mixture was allowed to cool to a room temperature and acidified with 2-N hydrochloric acid. The precipitated crystal was separated by filtration to give the title compound (90 mg, 95%).
Workup
- customobtained in the Step 18-1-2
- temperaturethe mixture was heated
- temperatureunder reflux
- customThe precipitated crystal was separated by filtration
Sources & evidence
- ORD record
- ord-aec7ffbcc74b4ac8b82762a3e3e78cce
- Source dataset
- uspto-grants-2015_12
- Patent number
- US09200008B2
Reaction notes
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