반응 #331398

ord-88036a6f56b14483833f9de99686b96f

시약

없음

용매

반응 조건

상세 조건
See reaction.notes.procedure_details.

후처리

  1. 1
    기타equipped with a reflux condenser
  2. 2
    기타was evacuated
  3. 3
    workup.ADDITIONrefilled with Ar several times
  4. 4
    온도the reaction mixture was heated
  5. 5
    온도to reflux under Ar for 5 h
  6. 6
    기타then partitioned between DCM (80 mL) and H2O (10 mL)
  7. 7
    추출The aqueous layer was extracted with DCM (1×)
  8. 8
    세척The combined organics were washed (brine)
  9. 9
    건조dried (Na2SO4)
  10. 10
    농축concentrated under reduced pressure

실험 절차

A flask containing 4,7-dichlorquinazoline (250 mg, 0.91 mmol) equipped with a reflux condenser was evacuated and refilled with Ar several times. MeONa (2 mL, 25% wt in MeOH, 8.7 mmol) and anh. MeOH (20 mL) were added and the reaction mixture was heated to reflux under Ar for 5 h. The reaction was cooled to rt and stored at rt overnight then partitioned between DCM (80 mL) and H2O (10 mL). The aqueous layer was extracted with DCM (1×). The combined organics were washed (brine), dried (Na2SO4) and concentrated under reduced pressure to provide the title compound as an off-white solid; 1H NMR (400 MHz, CDCl3) δ 8.55-8.62 (m, 2H), 8.08 (d, J=9.2 Hz, 1H), 7.99 (d, J=2.0 Hz, 1H), 7.52-7.48 (m, 3H), 7.45 (dd, J=2.0 Hz, 8.8 Hz, 1H), 4.28 (s, 3H).

출처

DOI: 10.6084/m9.figshare.5104873.v1특허: US08653268B2uspto-grants-2014_02