Sodium Hydroxide → 6-Chloro-4-phenyl-2-(2,2,2-trifluoro-ethoxy)-quinoline-3-carboxylic acid
Reaction equation
C([O:3][C:4]([C:6]1[C:7]([O:23][CH2:24][C:25]([F:28])([F:27])[F:26])=[N:8][C:9]2[C:14]([C:15]=1[C:16]1[CH:21]=[CH:20][CH:19]=[CH:18][CH:17]=1)=[CH:13][C:12]([Cl:22])=[CH:11][CH:10]=2)=[O:5])C.[OH-].[Na+]>C(O)C>[Cl:22][C:12]1[CH:13]=[C:14]2[C:9](=[CH:10][CH:11]=1)[N:8]=[C:7]([O:23][CH2:24][C:25]([F:28])([F:26])[F:27])[C:6]([C:4]([OH:5])=[O:3])=[C:15]2[C:16]1[CH:17]=[CH:18][CH:19]=[CH:20][CH:21]=1Participants
4
Reactant 2
Product 1
Reagents, catalysts & solvents 1
Procedure
The title compound was prepared in analogy to example 6 step B from a mixture of 6-chloro-4-phenyl-2-(2,2,2-trifluoro-ethoxy)-quinoline-3-carboxylic acid ethyl ester and 1N NaOH in ethanol. Off white solid (19.2 mg, 17%). LC-MS: 382 (M+H)+.
Sources & evidence
- ORD record
- ord-5dc338a422c84810b1c36c14b66709c2
- Source dataset
- uspto-grants-2015_12
- Patent number
- US09199938B2
Reaction notes
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