3-(2,4-Dichlorophenyl)-2,5-dimethylpyrazine 1-oxide → 3-(2,4-Dichlorophenyl)-2,5-diethylpyrazine 1-oxide
Reaction equation
ClC1C=C(Cl)C=CC=1C1C(C)=[N+]([O-:16])C=C(C)N=1.[Cl:18][C:19]1[CH:24]=[C:23]([Cl:25])[CH:22]=[CH:21][C:20]=1[C:26]1[C:27]([CH2:34][CH3:35])=[N:28][CH:29]=[C:30]([CH2:32][CH3:33])[N:31]=1>>[Cl:18][C:19]1[CH:24]=[C:23]([Cl:25])[CH:22]=[CH:21][C:20]=1[C:26]1[C:27]([CH2:34][CH3:35])=[N+:28]([O-:16])[CH:29]=[C:30]([CH2:32][CH3:33])[N:31]=1Participants
3
Procedure
Following the procedure of 3-(2,4-dichlorophenyl)-2,5-dimethylpyrazine 1-oxide but substituting Preparation of 3-(2,4-dichlorophenyl)-2,5-diethylpyrazine and making non-critical variations, the title compound was obtained (quantitative). It was used without preparation. 1H NMR (CDCl3) δ 1.12, 1.34, 2.55, 2.81, 2.89, 7.28, 7.40, 7.55, 8.11.
Sources & evidence
- ORD record
- ord-e30ac5ae2d9343b4baad2b72b7f9bce6
- Source dataset
- uspto-grants-2006_01
- Patent number
- US06992087B2
Reaction notes
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