2-(Chloromethyl)pyridine 1-oxide → HCID 178478899、化合物
反応式
[F:1][C:2]1[CH:7]=[CH:6][CH:5]=[C:4]([F:8])[C:3]=1[N:9]=[C:10]1[NH:14][CH2:13][CH2:12][N:11]1[OH:15].[Cl:16][CH2:17][C:18]1[CH:23]=[CH:22][CH:21]=[CH:20][N+:19]=1[O-:24].CC(C)=O.[ClH:29]>O1CCOCC1>[ClH:16].[ClH:29].[F:8][C:4]1[CH:5]=[CH:6][CH:7]=[C:2]([F:1])[C:3]=1[N:9]=[C:10]1[NH:14][CH2:13][CH2:12][N:11]1[O:15][CH2:17][C:18]1[CH:23]=[CH:22][CH:21]=[CH:20][N+:19]=1[O-:24]参加物
5
実験手順
From 2-[(2,6-difluorophenyl)imino]-1-hydroxy-imidazolidine and 2-chloromethyl-pyridine N-oxide there is obtained, in analogy to the details in Example 1,2-([{2-[(2,6-difluorophenyl)imino]-1-imidazolidinyl}oxy]methyl)-pyridine 1-oxide dihydrochloride of melting point 188°-189° (acetone/hydrogen chloride in dioxane).
出典と根拠
- ORDレコード
- ord-d75679cb844e4f339e7e79ce8ebfba31
- 出典データセット
- uspto-grants-1982_12
- 特許番号
- US04366160
反応ノート
読み込み中…