تفاعل #52940

ord-31e592cc2df741b490f935ebab442950

المذيبات

ظروف التفاعل

الظروف التفصيلية
See reaction.notes.procedure_details.

المعالجة

  1. 1
    درجة الحرارةthe mixture was refluxed for 1 day
  2. 2
    درجة الحرارةthe mixture was refluxed for another day
  3. 3
    تركيزThe mixture was then concentrated
  4. 4
    استخلاصextracted with CH2Cl2
  5. 5
    غسيلThe extract Was washed with sat. NaHCO3, water
  6. 6
    تجفيفdried (MgSO4)
  7. 7
    ترشيحfiltered
  8. 8
    أخرىevaporated
  9. 9
    أخرىThe residue was purified by preparative TLC (silica gel; eluent: hexane/AcOEt 5:1 to 2:1)

الإجراء التجريبي

N-(2,6-Dichlorobenzoyl)-4-(2,6-dimethoxyphenyl)-L-phenylalanine methyl ester (232 mg) was dissolved in anhydrous MeCN (10 mL) under N2 and 3,5-dichloro-1-fluoropyridinium triflate (85%, 353 mg) was added and the mixture was refluxed for 1 day. More 3,5-dichloro-1-fluoropyridinium triflate (175 mg) was added and the mixture was refluxed for another day. The mixture was then concentrated, and the residue was taken up with water and extracted with CH2Cl2. The extract Was washed with sat. NaHCO3, water, dried (MgSO4), filtered and evaporated. The residue was purified by preparative TLC (silica gel; eluent: hexane/AcOEt 5:1 to 2:1) to give N-(2,6-dichlorobenzoyl)-4-(2,6-dimethoxy-3-fluorophenyl)-L-phenylalanine methyl ester (109 mg) and N-(2,6-dichlorobenzoyl)-4-(2,6-dimethoxy-3,5-difluorophenyl)-L-phenylalanine methyl ester (37 mg).

المصدر

DOI: 10.6084/m9.figshare.5104873.v1براءة الاختراع: US06855843B2uspto-grants-2005_02