2,4-Dichloro-5,7-difluoro-3-methylquinoline → HCID 59631382, compound
Reaction equation
Cl[C:2]1[C:11]([CH3:12])=[C:10]([Cl:13])[C:9]2[C:4](=[CH:5][C:6]([F:15])=[CH:7][C:8]=2[F:14])[N:3]=1.[CH3:16][C:17]1[CH:18]=[CH:19][C:20]([S:26][CH3:27])=[C:21](B(O)O)[CH:22]=1>>[Cl:13][C:10]1[C:9]2[C:4](=[CH:5][C:6]([F:15])=[CH:7][C:8]=2[F:14])[N:3]=[C:2]([C:19]2[CH:18]=[C:17]([CH3:16])[CH:22]=[CH:21][C:20]=2[S:26][CH3:27])[C:11]=1[CH3:12]Participants
3
Procedure
Prepared according to procedure F using 2,4-dichloro-5,7-difluoro-3-methylquinoline (130 mg, 0.51 mmol) and 5-methyl-2-(methylthio)phenylboronic acid to give 4-chloro-5,7-difluoro-3-methyl-2-(5-methyl-2-(methylthio)phenyl)quinoline. Mass Spectrum (ESI) m/e=350.0 (M+1).
Workup
- customPrepared
Sources & evidence
- ORD record
- ord-ef8a98f6c3a444b7bb02d69a890a5927
- Source dataset
- uspto-grants-2014_07
- Patent number
- US08765940B2
Reaction notes
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