Azetidine → HCID 59612876, 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.[NH:12]1[CH2:15][CH2:14][CH2:13]1>>[N:12]1([C:2]2[N:7]=[C:6]([CH3:8])[C:5]([N+:9]([O-:11])=[O:10])=[CH:4][CH:3]=2)[CH2:15][CH2:14][CH2:13]1Participants
3
Procedure
Prepared from 6-chloro-2-methyl-3-nitropyridine and azetidine following the method used to prepare Intermediate 46. LCMS (ES+) 194 (M+H)+, RT 2.55 minutes (method 1).
Workup
- customLCMS (ES+) 194 (M+H)+, RT 2.55 minutes (method 1)
Sources & evidence
- ORD record
- ord-19c440045a154020a43d2035830620c8
- Source dataset
- uspto-grants-2015_08
- Patent number
- US09096614B2
Reaction notes
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