Flumazenil → ethyl 8-fluoro-5,6-dihydro-5-methyl-6-thioxo-4H-imidazo[1,5-a][1,4]benzodiazepine-3-carboxylate

HRID 67294

Reaktionsgleichung

Reaktionsgleichung von HRID 67294
[F:1][C:2]1[CH:3]=[CH:4][C:5]2[N:11]3[CH:12]=[N:13][C:14]([C:15]([O:17][CH2:18][CH3:19])=[O:16])=[C:10]3[CH2:9][N:8]([CH3:20])[C:7](=O)[C:6]=2[CH:22]=1.COC1C=CC(P2(=S)SP(=S)(C3C=CC(OC)=CC=3)[S:32]2)=CC=1>C1(C)C=CC=CC=1>[F:1][C:2]1[CH:3]=[CH:4][C:5]2[N:11]3[CH:12]=[N:13][C:14]([C:15]([O:17][CH2:18][CH3:19])=[O:16])=[C:10]3[CH2:9][N:8]([CH3:20])[C:7](=[S:32])[C:6]=2[CH:22]=1

Komponenten

4

Versuchsvorschrift

10.7 g (35.3 mmol) of ethyl 8-fluoro-5,6-dihydro-5-methyl-6-oxo-4H-imidazo[1,5-a][1,4]benzodiazepine-3-carboxylate and 7.13 g (17.6 mmol) of 2,4-bis(p-methoxyphenyl)-1,3,2,4-dithiadiphosphetane-2,4-disulphide in 100 ml of toluene are heated to boiling under reflux for 22 hours. The mixture is subsequently concentrated in vacuo until crystallisation begins and is then left to stand in an ice-bath for 1 hour. The crystallised-out material is filtered off under suction and washed with a small amount of toluene. The mixture is separated on silica gel with ethyl acetate/chloroform (1:9). After recrystallisation from ethyl acetate, there is obtained pure ethyl 8-fluoro-5,6-dihydro-5-methyl-6-thioxo-4H-imidazo[1,5-a][1,4]benzodiazepine-3-carboxylate of melting point 157°-159° C.

Aufarbeitung

  1. temperatureunder reflux for 22 hours
  2. concentrationThe mixture is subsequently concentrated in vacuo until crystallisation
  3. waitis then left
  4. filtrationThe crystallised-out material is filtered off under suction
  5. washwashed with a small amount of toluene
  6. customThe mixture is separated on silica gel with ethyl acetate/chloroform (1:9)
  7. customAfter recrystallisation from ethyl acetate

Quellen und Nachweise

ORD-Eintrag
ord-b84ca8c0e2f343cc8dfa43723674dc70
Quelldatensatz
uspto-grants-1982_08
Patentnummer
US04346030

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