تفاعل #4779
ord-f9e672f1e9b44c4186cfbb5036d7a208
معادلة التفاعل
الكواشف
المذيبات
ظروف التفاعل
المعالجة
- 1درجة الحرارةwas refluxed for 6 hours
- 2أخرىAfter evaporating the solvent
- 3workup.DISSOLUTIONthe residue was dissolved in chloroform
- 4غسيلwashed with saturated aqueous sodium chloride
- 5تجفيفdried over magnesium sulfate
- 6أخرىThe filtrate was evaporated under reduced pressure
- 7غسيلeluting with chloroform
- 8workup.ADDITIONThe fractions containing the object compound
- 9تركيزconcentrated under reduced pressure
- 10أخرىThe residue was recrystallized from diethyl ether
الإجراء التجريبي
A mixture of 5-bromomethyl-6-methyl-4-(3-nitrophenyl)-2-phenylpyrimidine (1.5 g), N-methylpiperazine (1.17 g) in isopropyl alcohol (15 ml) was refluxed for 6 hours. After evaporating the solvent, the residue was dissolved in chloroform, washed with saturated aqueous sodium chloride and dried over magnesium sulfate. The filtrate was evaporated under reduced pressure, and the residue was subjected to column chromatography on alumina (100 g) eluting with chloroform. The fractions containing the object compound were combined and concentrated under reduced pressure. The residue was recrystallized from diethyl ether to give 6-methyl-5-(4-methylpiperazin-1-ylmethyl)-4-(3-nitrophenyl)-2-phenylpyrimidine. (0.30 g).