Lithium Hydroxide → HCID 21266528, compound
Reaction equation
C([O:4][CH:5]1[NH:10][C:9](=[O:11])[CH:8]=[C:7]([C:12]2[CH:13]=[C:14]([CH3:18])[CH:15]=[CH:16][CH:17]=2)[CH:6]1[C:19]1[CH:24]=[CH:23][N:22]=[CH:21][CH:20]=1)(=O)C.[Li+].[OH-]>C1COCC1.O>[OH:4][CH:5]1[NH:10][C:9](=[O:11])[CH:8]=[C:7]([C:12]2[CH:13]=[C:14]([CH3:18])[CH:15]=[CH:16][CH:17]=2)[CH:6]1[C:19]1[CH:20]=[CH:21][N:22]=[CH:23][CH:24]=1Participants
5
Reactant 2
Product 1
Reagents, catalysts & solvents 2
Procedure
To a solution of 6-acetoxy-4-m-tolyl-5,6-dihydro-1H-[5,4′]bipyridinyl-2-one (200 mg, 0.6 mmole) in THF (2 mL) and water (2 mL) at r.t. was added LiOH (51 mg, 1.2 mmole) in one portion. The reaction mixture was stirred at that temperature for 10 min before quenching the mixture with aqueous NH4Cl. The reaction was quenched with 1.45 mL of 1N HCl the resulting white precipitate was filtered, rinsed with water and dried to give the title compound as a white solid.
Workup
- custombefore quenching the mixture with aqueous NH4Cl
- customThe reaction was quenched with 1.45 mL of 1N HCl the resulting white precipitate
- filtrationwas filtered
- washrinsed with water
- customdried
Sources & evidence
- ORD record
- ord-3ceb84deacad46f8b90e891aa15f82a6
- Source dataset
- uspto-grants-2001_01
- Patent number
- US06174901B1
Reaction notes
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