Potassium Hydroxide → HCID 17974489, compound
Reaction equation
[CH:1]([C:4]1[N:8]2[CH:9]=[C:10]([O:13][C:14]3[CH:26]=[CH:25][CH:24]=[CH:23][C:15]=3[CH2:16][O:17]C(=O)C(C)C)[CH:11]=[CH:12][C:7]2=[N:6][N:5]=1)([CH3:3])[CH3:2].[OH-].[K+]>O1CCCC1.O>[CH:1]([C:4]1[N:8]2[CH:9]=[C:10]([O:13][C:14]3[CH:26]=[CH:25][CH:24]=[CH:23][C:15]=3[CH2:16][OH:17])[CH:11]=[CH:12][C:7]2=[N:6][N:5]=1)([CH3:3])[CH3:2]Participants
5
Reactant 2
Product 1
Reagents, catalysts & solvents 2
Conditions
- Temperature
- 60 °C
Procedure
A mixture of isobutyric acid 2-(3-isopropyl-[1,2,4]triazolo[4,3-a]pyridin-6-yloxy)-benzyl ester (130 mg, 0.37 mmol) and potassium hydroxide (103 mg, 1.84 mmol) in tetrahydrofuran (6 mL) and water (1 mL) was heated at 60° C. for 7 hours. The reaction was concentrated in vacuo to a solid. The residue was suspended in water, the solid filtered, then the material suspended in methylene chloride and filtered to give the above named compound as a tan solid (84 mg, 80%).
Workup
- concentrationThe reaction was concentrated in vacuo to a solid
- filtrationthe solid filtered
- filtrationfiltered
- customto give the
Sources & evidence
- ORD record
- ord-bc7dea3272f94ea998fe6162b914ef3b
- Source dataset
- uspto-grants-2008_01
- Patent number
- US07321040B2
Reaction notes
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