تفاعل #349523

ord-b715ca919a7d4e58bd0e210d664b2ad6

معادلة التفاعل

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

المذيبات

ظروف التفاعل

الظروف التفصيلية
See reaction.notes.procedure_details.

المعالجة

  1. 1
    درجة الحرارةto reflux for 17 hours
  2. 2
    درجة الحرارةThe mixture was cooled
  3. 3
    ترشيحfiltered
  4. 4
    غسيلthe collected solids washed thoroughly with THF
  5. 5
    تركيزThe combined filtrate and washings were concentrated in vacuo
  6. 6
    أخرىRecrystallization of this crude product from THF/hexane
  7. 7
    أخرىyielded the desired end product
  8. 8
    أخرىwas obtained as colorless plates

الإجراء التجريبي

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°.

المصدر

DOI: 10.6084/m9.figshare.5104873.v1براءة الاختراع: US04153799uspto-grants-1979_05