Hydrochloric Acid → HCID 145734634, compound
Reaction equation
[OH-].[Na+].[CH2:3]([C:10]1[C:18]2[C:13](=[CH:14][C:15]([OH:23])=[C:16]([C:19]([O:21]C)=[O:20])[CH:17]=2)[NH:12][N:11]=1)[C:4]1[CH:9]=[CH:8][CH:7]=[CH:6][CH:5]=1.Cl>CO.O>[CH2:3]([C:10]1[C:18]2[C:13](=[CH:14][C:15]([OH:23])=[C:16]([C:19]([OH:21])=[O:20])[CH:17]=2)[NH:12][N:11]=1)[C:4]1[CH:5]=[CH:6][CH:7]=[CH:8][CH:9]=1Participants
6
Reactant 3
Product 1
Reagents, catalysts & solvents 2
Procedure
1.4 595 μl of 2 N NaOH are added to a suspension of 112 mg of “A1” in 1.5 ml of methanol, and the mixture is stirred at 60° for 3 hours. The mixture is cooled, 0.7 ml of 2 N HCl is added, the mixture is diluted with water, the precipitate is removed, and the mixture is subjected to conventional work-up, giving 75 mg of 3-benzyl-6-hydroxy-1H-indazole-5-carboxylic acid (“A2”).
Workup
- temperatureThe mixture is cooled
- customthe precipitate is removed
Sources & evidence
- ORD record
- ord-179e0d5d770b4722b2702536799b1ca9
- Source dataset
- uspto-grants-2014_05
- Patent number
- US08722903B2
Reaction notes
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