反応 #1065451

反応方程式

4-methyl-1,2-dihydrobenzo[c]pyrrolo[1,2,3-ef][1,5]benzodiazepin-7-one

N-methylpiperazine

→

product

4-Methyl-7-(4-methyl-1-piperazinyl)-1,2-dihydrobenzo[c]pyrrolo[1,2,3-ef][1,5]benzodiazepine

溶媒

Toluene

toluene

反応条件

後処理

1. 1
   温度The mixture was heated
2. 2
   温度under reflux for two hours
3. 3
   その他the insoluble material was removed by filtration
4. 4
   その他The organic phase was separated
5. 5
   抽出The aqueous phase was extracted with toluene (200 ml)
6. 6
   洗浄The combined toluene solutions were washed with water (300 ml), brine (2 times, 300 ml)
7. 7
   乾燥dried over anhydrous sodium sulfate
8. 8
   その他The solvent was evaporated
9. 9
   その他The residue was triturated with ethanol
10. 10
    その他Recrystallization of the solid from chloroform

実験手順

A solution of 4-methyl-1,2-dihydrobenzo[c]pyrrolo[1,2,3-ef][1,5]benzodiazepin-7-one (3.6 g, 14.3 mmoles), N-methylpiperazine (16 ml) and toluene (350 ml) was heated to 110° C. Titanium tetrachloride (4.3 ml) was added in three portions in two minute intervals. The mixture was heated under reflux for two hours and cooled to room temperature. Toluene (500 ml) and ice-water (500 m) were added. The mixture was stirred for 30 minutes and the insoluble material was removed by filtration. The organic phase was separated. The aqueous phase was extracted with toluene (200 ml). The combined toluene solutions were washed with water (300 ml), brine (2 times, 300 ml) and dried over anhydrous sodium sulfate. The solvent was evaporated. The residue was triturated with ethanol:hexane to a solid. Recrystallization of the solid from chloroform:hexane yielded 2.4 g of product. The mother liquor was concentrated and the residue was purified on a silica gel column (60 g, 230-400 mesh) to give a second crop of 1.3 g of product (77% overall yield). Recrystallization from 2-propanol gave the analytical sample, mp 173°-174° C.

出典