تفاعل #2258

ord-e95dea12efcf46abb4f2455c2c2c6569

معادلة التفاعل

COC(=O)c1cccc(Nc2nccc(-c3ccnc(NCCCO)c3)n2)c1
N-[3-methoxycarbonyl-phenyl]-4-[2-(3-hydroxy-propyl-amino)-4-pyridyl]-2-pyrimidineamine
NCCCN
1,3-diamino-propane
NCCCNC(=O)c1cccc(Nc2nccc(-c3ccnc(NCCCO)c3)n2)c1
N-[3-{N-(3-amino-propyl)-aminocarbonyl}-phenyl]-4-[2-(3-hydroxy-propyl-amino)-4-pyridyl]-2-pyrimidineamine

المذيبات

ظروف التفاعل

الظروف التفصيلية
See reaction.notes.procedure_details.

المعالجة

  1. 1
    استخلاصextracted with 2×10 ml of sodium chloride solution
  2. 2
    أخرىThe organic phase is dried
  3. 3
    تركيزconcentrated
  4. 4
    أخرىcrystallised from methylene chloride/diethyl ether

الإجراء التجريبي

100 mg (0.26 mmol) of N-[3-methoxycarbonyl-phenyl]-4-[2-(3-hydroxy-propyl-amino)-4-pyridyl]-2-pyrimidineamine and 0.5 ml of 1,3-diamino-propane are stirred for 24 h at 90° and then diluted with 20 ml of ethyl acetate and extracted with 2×10 ml of sodium chloride solution. The organic phase is dried, concentrated and crystallised from methylene chloride/diethyl ether to give N-[3-{N-(3-amino-propyl)-aminocarbonyl}-phenyl]-4-[2-(3-hydroxy-propyl-amino)-4-pyridyl]-2-pyrimidineamine;

المصدر

DOI: 10.6084/m9.figshare.5104873.v1براءة الاختراع: US05728708uspto-grants-1998_03