Imidazole → 2-(Imidazol-1-ylmethyl)-3-hydroxy-4-methylpyridine
反応式
[CH3:1][N:2]([CH2:4][C:5]1[C:10]([OH:11])=[C:9]([CH3:12])[CH:8]=[CH:7][N:6]=1)[CH3:3].[NH:13]1C=CN=[CH:14]1>C1(C)C(C)=CC=CC=1>[N:2]1([CH2:4][C:5]2[C:10]([OH:11])=[C:9]([CH3:12])[CH:8]=[CH:7][N:6]=2)[CH:1]=[CH:14][N:13]=[CH:3]1参加物
4
実験手順
The procedure described in Example 1 was then repeated except that 2-dimethylaminomethyl-3-hydroxy-4-methylpyridine (4.44 g.) and imidazole (1.82 g.) were reacted in xylene (15 ml.) to afford 2-(imidazol-1-ylmethyl)-3-hydroxy-4-methylpyridine (yield, 3.60 g.), m.p. 170°-172° C. after recrystallization from toluene.
出典と根拠
- ORDレコード
- ord-819b2155e7864cdfb09631673adb5f36
- 出典データセット
- uspto-grants-1980_10
- 特許番号
- US04230714
反応ノート
読み込み中…