反应详情
EQUATION
反应方程式
REACTANTS
反应物
PRODUCTS
生成物
AUXILIARIES
试剂、催化剂与溶剂
PROCEDURE
实验过程
The 2-(4-chlorophenyl)-3H-imidazo[4,5-b]pyridine (2.29 g, 0.01 mole), was added to a suspension of sodium hydride (0.44 g of 60% sodium hydride/oil, 0.01 mole, washed once with hexanes) in 50 ml of dimethylformamide. The mixture was heated to 70° C. for 1 hr before the addition of chloroacetone (0.93 g, 0.01 mole) at room temperature. The reaction mixture was stirred at room temperature overnight, then poured into 300 ml of water. The precipitate was collected by filtration, washed with water, and dried under high vacuum at 50° C. overnight. The solid was recrystallized from methanol-water and dried under high vacuum at 50° C. overnight. The solid was dissolved in methanol, treated with charcoal, and filtered through Celite to give a pale yellow filtrate. The filtrate was concentrated and diluted with water to initiate crystallization. The precipitate was collected by filtration, washed with water, and dried under high vacuum overnight. The solid was dissolved in isopropyl alcohol, acidified with ethereal hydrogen chloride, diluted with isopropyl ether, and seeded to initiate crystallization. The crystalline solid was collected by filtration, washed with isopropyl ether, and dried under high vacuum overnight to give 1.6 g (50%), m.p. 220°-22° C.
WORKUP
后处理
- washwashed once with hexanes) in 50 ml of dimethylformamide
- filtrationThe precipitate was collected by filtration
- washwashed with water
- customdried under high vacuum at 50° C. overnight
- customThe solid was recrystallized from methanol-water
- customdried under high vacuum at 50° C. overnight
- dissolutionThe solid was dissolved in methanol
- additiontreated with charcoal
- filtrationfiltered through Celite
- customto give a pale yellow filtrate
- concentrationThe filtrate was concentrated
- additiondiluted with water
- customcrystallization
- filtrationThe precipitate was collected by filtration
- washwashed with water
- customdried under high vacuum overnight
- dissolutionThe solid was dissolved in isopropyl alcohol
- additiondiluted with isopropyl ether
- customcrystallization
- filtrationThe crystalline solid was collected by filtration
- washwashed with isopropyl ether
- customdried under high vacuum overnight
- customto give 1.6 g (50%), m.p. 220°-22° C.