تفاعل #4780

ord-7f820da542c94a05a709cf0743a91157

المذيبات

ظروف التفاعل

الظروف التفصيلية
See reaction.notes.procedure_details.

المعالجة

  1. 1
    درجة الحرارةwas refluxed for 1.5 hours
  2. 2
    أخرىThe reaction mixture was evaporated in vacuo
  3. 3
    أخرىThe residue was chromatographed on allumina
  4. 4
    workup.ADDITIONeluting with a mixture of ethyl acetate and n-hexane (1:20)
  5. 5
    workup.ADDITIONThe fractions containing the desired product
  6. 6
    تركيزconcentrated in vacuo
  7. 7
    أخرىThe 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).

المصدر

DOI: 10.6084/m9.figshare.5104873.v1براءة الاختراع: US04727073uspto-grants-1988_02