Lithium Hydroxide → HCID 21101788, compound
Reaction equation
[Cl:1][C:2]1[CH:11]=[C:10]2[C:5]([C:6]([N:17]3[CH2:22][CH2:21][N:20]([C:23]([NH:25][C:26]4[CH:31]=[CH:30][C:29]([F:32])=[CH:28][CH:27]=4)=[O:24])[CH2:19][CH2:18]3)=[CH:7][C:8]([C:12]([O:14]CC)=[O:13])=[N:9]2)=[CH:4][CH:3]=1.[Li+].[OH-]>C1COCC1.O>[Cl:1][C:2]1[CH:11]=[C:10]2[C:5]([C:6]([N:17]3[CH2:22][CH2:21][N:20]([C:23]([NH:25][C:26]4[CH:31]=[CH:30][C:29]([F:32])=[CH:28][CH:27]=4)=[O:24])[CH2:19][CH2:18]3)=[CH:7][C:8]([C:12]([OH:14])=[O:13])=[N:9]2)=[CH:4][CH:3]=1Participants
4
Reactant 2
Product 1
Reagents, catalysts & solvents 1
Procedure
A solution of ethyl 7-chloro-4-[4-(4-fluorophenylaminocarbonyl)piperazin-1-yl]quinoline-2-carboxylate (389 mg, 0.85 mmol) in THF-water 3:1 (5 mL) is treated with LiOH x H2O (126 mg, 3 mmol) and stirred at room temp. for 4 h. The reaction mixture is concentrated and acidified with 1 N HCl (pH 4). The colorless precipitate is collected by filtration yielding the title product.
Workup
- concentrationThe reaction mixture is concentrated
- filtrationThe colorless precipitate is collected by filtration
Sources & evidence
- ORD record
- ord-21a4f4098449429d9c394651b1a5fb52
- Source dataset
- uspto-grants-2007_05
- Patent number
- US07220856B2
Reaction notes
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