반응 #349523

ord-b715ca919a7d4e58bd0e210d664b2ad6

반응 방정식

O=C1NC(c2ccccc2)c2cc(Cl)ccc2-n2nc(CO)cc21
end product
O=C1NC(c2ccccc2)c2cc(Cl)ccc2-n2nc(CO)cc21
8-Chloro-5,6-dihydro-4-oxo-6-phenyl-4H-pyrazolo[1,5-a][1,4]benzodiazepine-2-methanol
C1CCOC1
THF
O=Cc1cc2n(n1)-c1ccc(Cl)cc1C(c1ccccc1)NC2=O
8-Chloro-5,6-dihydro-4-oxo-6-phenyl-4H-pyrazolo[1,5-a][1,4]benzodiazepine-2-carboxaldehyde

반응 조건

상세 조건
See reaction.notes.procedure_details.

후처리

  1. 1
    온도to reflux for 17 hours
  2. 2
    온도The mixture was cooled
  3. 3
    여과filtered
  4. 4
    세척the collected solids washed thoroughly with THF
  5. 5
    농축The combined filtrate and washings were concentrated in vacuo
  6. 6
    기타Recrystallization of this crude product from THF/hexane
  7. 7
    기타yielded the desired end product
  8. 8
    기타was obtained as colorless plates

실험 절차

A solution of 5.85 g. (17 mmol) of the end product of Example 14 in 600 ml. dry THF was mixed with 24 g. of activated MnO2 and heated to reflux for 17 hours. The mixture was cooled, filtered and the collected solids washed thoroughly with THF. The combined filtrate and washings were concentrated in vacuo. Recrystallization of this crude product from THF/hexane yielded the desired end product. An analytical sample was prepared by an additional recrystallization from THF/hexane and was obtained as colorless plates: mp 276°-278°.

출처

DOI: 10.6084/m9.figshare.5104873.v1특허: US04153799uspto-grants-1979_05