1-Methyl-5-nitro-1H-imidazole-2-carbaldehyde → N-methyl-1-(1-methyl-5-nitroimidazol-2-yl)methanimine oxide
反応式
[CH3:1][N:2]1[C:6]([N+:7]([O-:9])=[O:8])=[CH:5][N:4]=[C:3]1[CH:10]=[N+:11]([CH2:13]C1C=CC=CC=1)[O-:12].Cl.C(NO)C1C=CC=CC=1.CN1C([N+]([O-])=O)=CN=C1C=O>>[CH3:1][N:2]1[C:6]([N+:7]([O-:9])=[O:8])=[CH:5][N:4]=[C:3]1[CH:10]=[N+:11]([CH3:13])[O-:12]参加物
4
実験手順
The corresponding α-(1-methyl-5-nitroimidazol-2-yl)-N-benzylnitrone can also be prepared using N-benzylhydroxylamine hydrochloride in the above reaction with 1-methyl-2-formyl-5-nitroimidazole.
出典と根拠
- ORDレコード
- ord-f4c1d66eaf1e42f4907d760df652e0e2
- 出典データセット
- uspto-grants-1978_03
- 特許番号
- US04080340
反応ノート
読み込み中…