HCID 18966371, compound → HCID 86748131, compound
Reaction equation
[CH:1]([C:3]1[N:8]=[C:7]([C:9]2[CH:14]=[CH:13][CH:12]=[C:11]([CH3:15])[N:10]=2)[N:6]=[C:5]([CH3:16])[CH:4]=1)=[O:2].[Cl-].[CH2:18]([O:22][NH3+:23])[CH2:19][CH2:20][CH3:21]>>[CH:1]([C:3]1[C:4](=[N:23][O:22][CH2:18][CH2:19][CH2:20][CH3:21])[CH:5]([CH3:16])[N:6]=[C:7]([C:9]2[CH:14]=[CH:13][CH:12]=[C:11]([CH3:15])[N:10]=2)[N:8]=1)=[O:2]Participants
3
Procedure
If 6-formyl-4-methyl-2-(6-methyl-2-pyridyl)pyrimidine is used instead of 4-formyl-2-(2-pyridyl)pyrimidine and O-n-butylhydroxylammonium chloride instead of hydroxylammonium chloride, 6-formyl-O-n-butyloximino-4-methyl-2-(6-methyl-2-pyridyl)-pyrimidine (compound 133c) is obtained in a corresponding manner.
Sources & evidence
- ORD record
- ord-85da2a4c764a4b02929b0ea0056784fe
- Source dataset
- uspto-grants-1994_09
- Patent number
- US05346899
Reaction notes
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