تفاعل #4271
ord-6577de97230742bfbdfb63b5e64d45dc
معادلة التفاعل
المتفاعلات
الكواشف
ظروف التفاعل
المعالجة
- 1درجة الحرارةis refluxed for 2 hours
- 2ترشيحis filtered over activated charcoal
- 3أخرىto remove the insoluble components
- 4أخرىthe filtrate is evaporated to dryness in vacuo
- 5أخرىIn order to purify it
- 6ترشيحThe insoluble matter is filtered off
- 7workup.ADDITIONby the addition of potassium carbonate
- 8أخرىthe resin precipitated
- 9تجفيفAfter drying over magnesium sulphate
- 10أخرىthe solution is evaporated to dryness in vacuo
- 11ترشيحfiltered
- 12درجة الحرارةafter cooling
- 13أخرىis obtained which melts at 212° to 214° C.
- 14غسيلafter washing with ether
الإجراء التجريبي
A reaction mixture consisting of 36.6 g (0.12 mol) of 5,11-dihydro-11-[1-oxo-2-methyl-4-pentynyl]-6H-pyrido[2,3-b][1,4]benzodiazepin-6-one, 4 g (0.13 mol) of paraformaldehyde, 13.2 g (0.13 mol) of N-methylpiperazine, 0.2 g of copper(I) chloride and 600 ml of dioxan is refluxed for 2 hours. After the reaction has ended the mixture is filtered over activated charcoal to remove the insoluble components and the filtrate is evaporated to dryness in vacuo. In order to purify it, the crude product is suspended in a solution of 15.4 g (0.13 mol) of maleic acid in 600 ml of water and stirred for 1 hour at ambient temperature. The insoluble matter is filtered off, the filtrate is made alkaline by the addition of potassium carbonate and the resin precipitated is taken up in 600 ml of methylene chloride. After drying over magnesium sulphate, the solution is evaporated to dryness in vacuo. The crystalline residue is decocted with 150 ml of ethyl acetate and suction filtered after cooling. By digesting it in a little ethyl acetate a crystalline product is obtained which melts at 212° to 214° C. after washing with ether.