Реакция #156564

ord-83e1e50720b94f12a0eb84c9f1eddbd2

Растворители

Условия реакции

Подробные условия
See reaction.notes.procedure_details.

Обработка

  1. 1
    Температураheated
  2. 2
    Температураto reflux overnight under argon
  3. 3
    ДругоеThen, the solvent was removed under reduced pressure
  4. 4
    workup.STIRRINGThe residue solid was stirred in 100 mL of saturated K2CO3 solution
  5. 5
    ФильтрацияThe white solid was filtered out
  6. 6
    Другоеdried under vacuum
  7. 7
    Экстракцияextracted with CH2Cl2/MeOH (7/3 v/v) three times (100 mL)
  8. 8
    КонцентрированиеThe extracts were concentrated to dryness
  9. 9
    ДругоеThe residue was purified by column chromatography (silica-gel, CH2Cl2/MeOH=9/1 v/v)
  10. 10
    Другоеto give a pale-yellow solid product, 0.28 g, 82.8% yield

Методика

2-(4-(1-(5-Fluoro-2-methylphenyl)propan-2-ylamino)-2-oxo-1,2-dihydropyridin-3-yl)-6-methyl imidazo[4,5-f]isoindole-5,7(1H,6H)-dione (0.35 g, 0.76 mmol) and zinc powder (1.20 g, 18.28 mmol) were suspended in acetic acid (30 mL). The reaction mixture was stirred and heated to reflux overnight under argon. Then, the solvent was removed under reduced pressure. The residue solid was stirred in 100 mL of saturated K2CO3 solution. The white solid was filtered out, dried under vacuum and extracted with CH2Cl2/MeOH (7/3 v/v) three times (100 mL). The extracts were concentrated to dryness. The residue was purified by column chromatography (silica-gel, CH2Cl2/MeOH=9/1 v/v) to give a pale-yellow solid product, 0.28 g, 82.8% yield. MS: 444.0 [M−H]−. 1H-NMR (DMSO-d6, 300 MHz): δ 13.06 (s, 1H), 11.16 (s, 1H), 11.09-11.06 (m, 1H), 7.95 (s, 0.5H), 7.85 (s, 0.5H), 7.78 (s, 0.5H), 7.69 (s, 0.5H), 7.30-7.10 (m, 3H), 6.91-6.83 (m, 1H), 6.14-6.10 (m, 1H), 4.48 (s, 2H), 4.17-4.13 (m, 1H), 3.10 (s, 3H), 3.03-2.96 (m, 2H), 2.35 (d, 3H, J=4.9 Hz), 1.34-1.32 (m, 3H).

Источник

DOI: 10.6084/m9.figshare.5104873.v1Патент: US08822500B2uspto-grants-2014_09