HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1606953Erstellt: 25. Oktober 2026
Sodium amide → 7-chloro-3-[(Z)-2-chlorovinyl]-4,5-dihydro-5-methyl-6H-imidazo[1,5-a][1,4]benzodiazepin-6-one
https://huagongshe.com/reaction/1606953
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
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| Edukt | Sodium amide | HCID 24533 | — |
| Edukt | (Chloromethyl)triphenylphosphonium chloride | HCID 197823 | — |
| Edukt | 7-chloro-5,6-dihydro-5-methyl-6-oxo-4H-imidazo[1,5-a][1,4]benzodiazepine-3-carboxaldehyde | HCID 19851584 | — |
| Lösungsmittel | Tetrahydrofuran | HCID 8028 | — |
| Produkt | 7-chloro-3-[(Z)-2-chlorovinyl]-4,5-dihydro-5-methyl-6H-imidazo[1,5-a][1,4]benzodiazepin-6-one | HCID 86743355 | — |
Reaktionsschritte
100 g of an equimolar mixture of chloromethyltriphenylphosphonium chloride and sodium amide were stirred for 45 minutes in 450 ml of tetrahydrofuran, whereby the temperature rose to 37°. 62.23 g (229.7 mmol) of 7-chloro-5,6-dihydro-5-methyl-6-oxo-4H-imidazo[1,5-a][1,4]benzodiazepine-3-carboxaldehyde were then added portionwise thereto at room temperature and, after completion of the addition, the mixture was stirred for a further 1 hour. The reaction mixture was subsequently filtered and the filtrate was evaporated. After chromatography of the residue on silica gel while eluting with cyclohexane/ether/wasopropanol (3:3:1) there was obtained 7-chloro-3-[(Z)-2-chlorovinyl]-4,5-dihydro-5-methyl-6H-imidazo[1,5-a][1,4]benzodiazepin-6-one of melting point 205°-207°.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US04863920 |
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| Quelldatensatz | uspto-grants-1989_09 |
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| ORD ID | ord-4e6d176c92604bb192e57a7ddecd8b8f |
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| Quellennotiz | uspto-grants-1989_09 |
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