2-Acetylpyridine → HCID 57901748, compound
Reaction equation
Cl.[N+:2]([C:5]1[CH:10]=[CH:9][CH:8]=[CH:7][C:6]=1[NH:11]N)([O-:4])=[O:3].[C:13]([C:16]1[CH:21]=[CH:20][CH:19]=[CH:18][N:17]=1)(=O)[CH3:14]>>[N+:2]([C:5]1[CH:10]=[CH:9][CH:8]=[C:7]2[C:6]=1[NH:11][C:13]([C:16]1[CH:21]=[CH:20][CH:19]=[CH:18][N:17]=1)=[CH:14]2)([O-:4])=[O:3]Participants
3
Procedure
2-Nitrophenylhydrazine hydrochloride (5 g, 26 mmol) and 2-acetylpyridine (2.5 ml, 26 mmol) were reacted according to the same procedures as Preparations 4 to 5 to give the title compound (1 g, Yield 16%).
Sources & evidence
- ORD record
- ord-4eb128ab97214435a40284100edad017
- Source dataset
- uspto-grants-2013_01
- Patent number
- US08349885B2
Reaction notes
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