6-Chloro-2-methyl-3-nitropyridine → HCID 89559048, compound
Reaction equation
Cl[C:2]1[N:7]=[C:6]([CH3:8])[C:5]([N+:9]([O-:11])=[O:10])=[CH:4][CH:3]=1.[F:12][CH:13]1[CH2:17][CH2:16][NH:15][CH2:14]1>>[F:12][CH:13]1[CH2:17][CH2:16][N:15]([C:2]2[N:7]=[C:6]([CH3:8])[C:5]([N+:9]([O-:11])=[O:10])=[CH:4][CH:3]=2)[CH2:14]1Participants
3
Procedure
The title compound was prepared from 6-chloro-2-methyl-3-nitropyridine and 3-fluoropyrrolidine following the method used to prepare Intermediate 51. LCMS (ES+) 226 (M+H)+, RT 2.847 minutes (method 1).
Workup
- customLCMS (ES+) 226 (M+H)+, RT 2.847 minutes (method 1)
Sources & evidence
- ORD record
- ord-0ec4ea6ff77d4ad28f3195f50320851e
- Source dataset
- uspto-grants-2015_08
- Patent number
- US09096614B2
Reaction notes
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