HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 443793Erstellt: 24. Oktober 2026
Pyridine → 1-methyl-7-chloro-3-dipropylacetoxy-5-phenyl-1,3-dihydro-2H-1,4-benzodiazepine-2-one
https://huagongshe.com/de/reaction/443793
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Pyridine | HCID 1049 | — |
| Edukt | Temazepam | HCID 5391 | — |
| Edukt | 2-Propylvaleryl chloride | HCID 76240 | — |
| Lösungsmittel | Dimethylformamide | HCID 6228 | — |
| Produkt | 1-methyl-7-chloro-3-dipropylacetoxy-5-phenyl-1,3-dihydro-2H-1,4-benzodiazepine-2-one | HCID 23465564 | — |
Reaktionsschritte
A solution of 15 g of 1-methyl-7-chloro-3-hydroxy-5-phenyl-1,3-dihydro-2H-1,4-benzodiazepine-2-one (Temazepam) and 5 g of absolute pyridine is cooled in 40 ml of freshly distilled dimethyl formamide to -5° and is mixed drop by drop with 10.5 g of dipropyl acetic acid chloride with the exclusion of atmospheric moisture. The mixture is stirred for an additional 4 hours at -5° and is allowed to stand over night at 0°, and then the mixture is poured on ice. The separated oil crystallizes while rubbed on with ethanol. By recrystallization from petroleum ether or isopropanol using activated charcoal, one will obtain the 1-methyl-7-chloro-3-dipropylacetoxy-5-phenyl-1,3-dihydro-2H-1,4-benzodiazepine-2-one as a colorless powder with a melting point of 134°-136°.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US04261987 |
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| Quelldatensatz | uspto-grants-1981_04 |
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| ORD ID | ord-b58383cd293c40228718e3d99a150283 |
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| Quellennotiz | uspto-grants-1981_04 |
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