Acetonitrile → 1-Benzyl-6-chloroimidazo[1,2-a]pyridinium bromide
反応式
[Cl:1][C:2]1[CH:3]=[CH:4][C:5]2[N:6]([CH:8]=[CH:9][N:10]=2)[CH:7]=1.[Br:11][CH2:12][C:13]1[CH:18]=[CH:17][CH:16]=[CH:15][CH:14]=1.C(#N)C>C(OCC)C>[Br-:11].[CH2:12]([N+:10]1[CH:9]=[CH:8][N:6]2[CH:7]=[C:2]([Cl:1])[CH:3]=[CH:4][C:5]=12)[C:13]1[CH:18]=[CH:17][CH:16]=[CH:15][CH:14]=1参加物
5
実験手順
A solution of 2.3 g. of 6-chloroimidazo[1,2-a]pyridine and 3.42 g. of α-bromotoluene in 40 ml. of dry acetonitrile is heated at reflux temperatures overnight. The solution is cooled and 35 ml. of diethyl ether added. The precipitated solids are collected and twice recrystallized from isopropanoldiethyl ether, 3.8 g., m.p. 193°-195° C.
後処理
- temperatureat reflux temperatures overnight
- temperatureThe solution is cooled
- customThe precipitated solids are collected
- customtwice recrystallized from isopropanoldiethyl ether, 3.8 g
出典と根拠
- ORDレコード
- ord-4a558a2e1a1247f3bd3d04709be73c04
- 出典データセット
- uspto-grants-1979_02
- 特許番号
- US04141898
反応ノート
読み込み中…