Tetrahydrofuran → 8-Chloro-5,6-dihydro-4-oxo-6-phenyl-4H-pyrazolo[1,5-a][1,4]benzodiazepine-2-carboxaldehyde

HRID 262341

Reaktionsgleichung

Reaktionsgleichung von HRID 262341
[Cl:1][C:2]1[CH:3]=[CH:4][C:5]2[N:11]3[N:12]=[C:13]([CH2:15][OH:16])[CH:14]=[C:10]3[C:9](=[O:17])[NH:8][CH:7]([C:18]3[CH:23]=[CH:22][CH:21]=[CH:20][CH:19]=3)[C:6]=2[CH:24]=1.C1COCC1>O=[Mn]=O.C1COCC1.CCCCCC>[Cl:1][C:2]1[CH:3]=[CH:4][C:5]2[N:11]3[N:12]=[C:13]([CH:15]=[O:16])[CH:14]=[C:10]3[C:9](=[O:17])[NH:8][CH:7]([C:18]3[CH:23]=[CH:22][CH:21]=[CH:20][CH:19]=3)[C:6]=2[CH:24]=1

Komponenten

5

Versuchsvorschrift

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°.

Aufarbeitung

  1. temperatureto reflux for 17 hours
  2. temperatureThe mixture was cooled
  3. filtrationfiltered
  4. washthe collected solids washed thoroughly with THF
  5. concentrationThe combined filtrate and washings were concentrated in vacuo
  6. customRecrystallization of this crude product from THF/hexane
  7. customyielded the desired end product
  8. customwas obtained as colorless plates

Quellen und Nachweise

ORD-Eintrag
ord-b715ca919a7d4e58bd0e210d664b2ad6
Quelldatensatz
uspto-grants-1979_05
Patentnummer
US04153799

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