Morpholine → 4-(4-Chloro-5,7-difluoro-3-methylquinolin-2-yl)morpholine
Reaction equation
[Cl:1][C:2]1[C:11]2[C:6](=[CH:7][C:8]([F:13])=[CH:9][C:10]=2[F:12])[N:5]=[C:4](C2C=CC=CC=2S(C)(=O)=O)[C:3]=1[CH3:24].[NH:25]1[CH2:30][CH2:29][O:28][CH2:27][CH2:26]1>>[Cl:1][C:2]1[C:11]2[C:6](=[CH:7][C:8]([F:13])=[CH:9][C:10]=2[F:12])[N:5]=[C:4]([N:25]2[CH2:30][CH2:29][O:28][CH2:27][CH2:26]2)[C:3]=1[CH3:24]Participants
3
Procedure
Essentially prepared according to Procedure G using 4-chloro-5,7-difluoro-3-methyl-2-(2-(methylsulfonyl)phenyl)quinoline (380.0 mg, 1.50 mmol) and morpholine to give 4-(4-chloro-5,7-difluoro-3-methylquinolin-2-yl)morpholine. Mass Spectrum (ESI) m/e=299.0 (M+1).
Workup
- customEssentially prepared
Sources & evidence
- ORD record
- ord-be764f89e70d4993a8cff576c587117c
- Source dataset
- uspto-grants-2015_01
- Patent number
- US08940724B2
Reaction notes
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