Acetylpyrazine → HCID 59576164, compound
Reaction equation
Cl.[CH3:2][C:3]1[CH:8]=[CH:7][C:6]([NH:9]N)=[C:5]([N+:11]([O-:13])=[O:12])[CH:4]=1.[C:14]([C:17]1[CH:22]=[N:21][CH:20]=[CH:19][N:18]=1)(=O)[CH3:15]>>[CH3:2][C:3]1[CH:8]=[C:7]2[C:6](=[C:5]([N+:11]([O-:13])=[O:12])[CH:4]=1)[NH:9][C:14]([C:17]1[CH:22]=[N:21][CH:20]=[CH:19][N:18]=1)=[CH:15]2Participants
3
Procedure
(4-Methyl-2-nitrophenyl)hydrazine hydrochloride (2 g, 9.8 mmol) and 2-acetylpyrazine (1.2 ml, 9.8 mmol) were reacted according to the same procedures as Preparations 4 to 5 to give the title compound (0.3 g, Yield 19%).
Sources & evidence
- ORD record
- ord-e8baa992e1bc4cc89357226a99ea2579
- Source dataset
- uspto-grants-2013_01
- Patent number
- US08349885B2
Reaction notes
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