HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 67294Erstellt: 23. Oktober 2026
Flumazenil → ethyl 8-fluoro-5,6-dihydro-5-methyl-6-thioxo-4H-imidazo[1,5-a][1,4]benzodiazepine-3-carboxylate
https://huagongshe.com/de/reaction/67294
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
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| Edukt | Flumazenil | HCID 3373 | — |
| Edukt | Lawesson's reagent | HCID 87949 | — |
| Lösungsmittel | Toluene | HCID 1140 | — |
| Produkt | ethyl 8-fluoro-5,6-dihydro-5-methyl-6-thioxo-4H-imidazo[1,5-a][1,4]benzodiazepine-3-carboxylate | HCID 20515334 | — |
Reaktionsschritte
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.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US04346030 |
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| Quelldatensatz | uspto-grants-1982_08 |
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| ORD ID | ord-b84ca8c0e2f343cc8dfa43723674dc70 |
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| Quellennotiz | uspto-grants-1982_08 |
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