반응 #89820

ord-35444501c9bd41b9adf690c071d44619

용매

반응 조건

상세 조건
See reaction.notes.procedure_details.

후처리

  1. 1
    기타Reaction mixture
  2. 2
    온도was refluxed for 2 h
  3. 3
    농축concentrated in vacuo
  4. 4
    workup.DISSOLUTIONThe residue was dissolved in EtOAc
  5. 5
    추출extracted with H2O (3×)
  6. 6
    기타Dried the organic layer under Na2SO4
  7. 7
    농축concentrated in vacuo
  8. 8
    추출extracted with CHCl3 (3×)
  9. 9
    기타dried under Na2SO4
  10. 10
    농축concentrated in vacuo

실험 절차

To a suspension of tert-butyl 5-(2-(3-((R)-1-(2,2,2-trifluoroacetyl)-pyrrolidine-2-carboxamido)phenyl)quinazolin-4-ylamino)-1H-indazole-1-carboxylate (100 mg, 0.15 mmol) in MeOH (5.7 mL) and H2O (345 mL) was added K2CO3 (108 mg, 0.78 mmol). Reaction mixture was refluxed for 2 h. Cooled to RT temperature and concentrated in vacuo. The residue was dissolved in EtOAc and extracted with H2O (3×). Dried the organic layer under Na2SO4 and concentrated in vacuo. The aqueous layer was basicified with 1 N NaOH, extracted with CHCl3 (3×), dried under Na2SO4 and concentrated in vacuo. The two organic layers were combined to afford tert-butyl 5-(2-(3-((R)-pyrrolidine-2-carboxamido)phenyl)quinazolin-4-ylamino)-1H-indazole-1-carboxylate. (65 mg, 79%).

출처

DOI: 10.6084/m9.figshare.5104873.v1특허: US09440961B2uspto-grants-2016_09