Hydrochloric Acid → HCID 83636313, compound
Reaction equation
[CH:1]([C:4]1[CH:8]=[C:7]([CH3:9])[N:6]([CH2:10][C:11]([O:13]CC)=[O:12])[N:5]=1)([CH3:3])[CH3:2].[Li+].[OH-].Cl>O>[CH:1]([C:4]1[CH:8]=[C:7]([CH3:9])[N:6]([CH2:10][C:11]([OH:13])=[O:12])[N:5]=1)([CH3:3])[CH3:2]Participants
5
Reactant 3
Product 1
Reagents, catalysts & solvents 1
Procedure
A mixture of ethyl (3-isopropyl-5-methyl-1H-pyrazol-1-yl)acetate (Preparation 129, 571 mg, 2.72 mmol) and LiOH (342 mg, 8.15 mmol) in IMS (5 mL) and water (4 mL) was stirred at room temperature for 30 minutes. The reaction was acidified with 2M HCl and extracted with EtOAc. The organic layer was collected, washed with brine, dried over MgSO4 and concentrated in vacuo to afford the title compound as a cream solid (328 mg, 66%).
Workup
- extractionextracted with EtOAc
- customThe organic layer was collected
- washwashed with brine
- dry with materialdried over MgSO4
- concentrationconcentrated in vacuo
Sources & evidence
- ORD record
- ord-82227e3321884828bf8997111878a266
- Source dataset
- uspto-grants-2015_10
- Patent number
- US09163021B2
Reaction notes
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