Lithium Hydroxide → HCID 59363504, compound
Reaction equation
[CH3:1][N:2]1[CH:6]=[C:5]([NH:7][C:8]([NH:10][C:11]2[CH:16]=[CH:15][C:14]([O:17][C:18]([F:21])([F:20])[F:19])=[CH:13][CH:12]=2)=[O:9])[CH:4]=[C:3]1[C:22]([O:24]CC)=[O:23].[OH-].[Li+]>C1COCC1.O>[CH3:1][N:2]1[CH:6]=[C:5]([NH:7][C:8]([NH:10][C:11]2[CH:12]=[CH:13][C:14]([O:17][C:18]([F:20])([F:21])[F:19])=[CH:15][CH:16]=2)=[O:9])[CH:4]=[C:3]1[C:22]([OH:24])=[O:23]Participants
5
Reactant 2
Product 1
Reagents, catalysts & solvents 2
Procedure
470 mg (1.27 mmol) of ethyl 1-methyl-4-[({[4-(trifluoromethoxy)phenyl]amino}carbonyl)amino]-1H-pyrrole-2-carboxylate are initially charged in 5 ml of THF, 152 mg (6.33 mmol) of lithium hydroxide in 1 ml of water are added and the mixture is stirred under reflux overnight. The reaction mixture is concentrated, the residue is acidified with 2M hydrochloric acid and the precipitate formed is filtered off with suction and dried under reduced pressure. This gives a solid.
Workup
- temperatureunder reflux overnight
- concentrationThe reaction mixture is concentrated
- customthe precipitate formed
- filtrationis filtered off with suction
- customdried under reduced pressure
- customThis gives a solid
Sources & evidence
- ORD record
- ord-ca89fc13e2a14b1f8278ccb967f19dcb
- Source dataset
- uspto-grants-2013_04
- Patent number
- US08410090B2
Reaction notes
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