تفاعل #4780
ord-7f820da542c94a05a709cf0743a91157
معادلة التفاعل
الكواشف
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المذيبات
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الظروف التفصيلية
See reaction.notes.procedure_details.
المعالجة
- 1درجة الحرارةwas refluxed for 1.5 hours
- 2أخرىThe reaction mixture was evaporated in vacuo
- 3أخرىThe residue was chromatographed on allumina
- 4workup.ADDITIONeluting with a mixture of ethyl acetate and n-hexane (1:20)
- 5workup.ADDITIONThe fractions containing the desired product
- 6تركيزconcentrated in vacuo
- 7أخرىThe residue was crystallized from a mixture of n-hexane and diethyl ether
الإجراء التجريبي
A mixture of 5-(1-bromoethyl)-6-methyl-4-(3-nitrophenyl)-2-phenylpyrimidine (1.5 g) and N-methylpiperazine (1.13 g) in isopropylalcohol (15 ml) was refluxed for 1.5 hours. The reaction mixture was evaporated in vacuo. The residue was chromatographed on allumina eluting with a mixture of ethyl acetate and n-hexane (1:20). The fractions containing the desired product were combined and concentrated in vacuo. The residue was crystallized from a mixture of n-hexane and diethyl ether to give 6-methyl-5-[1-(4-methylpiperazin-1-yl)ethyl]-4-(3-nitrophenyl)-2-phenylpyrimidine (0.51 g).