Hydrochloric Acid → HCID 71555919, compound
Reaction equation
C([O:5][C:6]([C:8]1[C:9]([O:28][CH:29]([CH3:34])[C:30]([F:33])([F:32])[F:31])=[N:10][C:11]2[C:16]([C:17]=1[C:18]1[CH:23]=[CH:22][CH:21]=[C:20]([CH:24]([CH3:26])[CH3:25])[CH:19]=1)=[CH:15][C:14]([Cl:27])=[CH:13][CH:12]=2)=[O:7])(C)(C)C.Cl>O1CCOCC1>[Cl:27][C:14]1[CH:15]=[C:16]2[C:11](=[CH:12][CH:13]=1)[N:10]=[C:9]([O:28][CH:29]([CH3:34])[C:30]([F:33])([F:31])[F:32])[C:8]([C:6]([OH:7])=[O:5])=[C:17]2[C:18]1[CH:23]=[CH:22][CH:21]=[C:20]([CH:24]([CH3:26])[CH3:25])[CH:19]=1Participants
4
Reactant 2
Product 1
Reagents, catalysts & solvents 1
Procedure
The title compound was prepared in analogy to example 78 step E from 6-chloro-4-(3-isopropyl-phenyl)-2-(2,2,2-trifluoro-1-methyl-ethoxy)-quinoline-3-carboxylic acid tert-butyl ester (70 mg, 0.14 mmol) and 4N HCl in dioxane. Off white solid (44 mg, 71%). LC-MS (ESI): 438 (M+H)+.
Sources & evidence
- ORD record
- ord-d47464d581cd47bb8bc114dde82429cf
- Source dataset
- uspto-grants-2015_12
- Patent number
- US09199938B2
Reaction notes
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