تفاعل #72800

ord-c497d058a0b34b9f8363e1ebb4347e19

الكواشف

لا شيء

ظروف التفاعل

الظروف التفصيلية
See reaction.notes.procedure_details.

المعالجة

  1. 1
    درجة الحرارةwas heated
  2. 2
    درجة الحرارةat reflux temperature for 8 h
  3. 3
    أخرىconsumption of starting material
  4. 4
    أخرىthe solvent was removed in-vacuo
  5. 5
    workup.ADDITIONThe residue was diluted with aqueous NaHCO3
  6. 6
    استخلاصextracted with EtOAc (250 mL×3)
  7. 7
    غسيلThe combined organic layers were washed with brine (250 mL×2)
  8. 8
    تجفيفdried over anhydrous Na2SO4
  9. 9
    ترشيحAfter filtration
  10. 10
    أخرىthe solvent was removed by rotary evaporator
  11. 11
    أخرىThe residue was then purified by silica gel chromatography
  12. 12
    غسيلeluted with EtOAc

الإجراء التجريبي

A mixture of methyl 2,3-diamino-5-(4-morpholinyl)benzoate (4.0 g) in CF3COOH (20 mL) was heated at reflux temperature for 8 h. When TLC analysis indicated consumption of starting material, the mixture was cooled to room temperature and the solvent was removed in-vacuo. The residue was diluted with aqueous NaHCO3 and extracted with EtOAc (250 mL×3). The combined organic layers were washed with brine (250 mL×2), dried over anhydrous Na2SO4. After filtration, the solvent was removed by rotary evaporator. The residue was then purified by silica gel chromatography eluted with EtOAc:petroleum ether=1:4 to afford the desired product as a pale solid. (4.3 g, 82.7%). 1H NMR (300 MHz, DMSO-d6): δ ppm 13.47 (s, 1H), 7.71 (s, 1H), 7.56 (s, 1H), 3.96 (s, 3H), 3.79 (t, 4H, J=4.5 Hz), 3.17 (s, 4H). LC-MS: m/e=330.1 [M+1]+.

المصدر

DOI: 10.6084/m9.figshare.5104873.v1براءة الاختراع: US08541411B2uspto-grants-2013_09