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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 441398Erstellt: 24. Oktober 2026

Methyl iodide → 1H-1,4-Benzodiazepine

https://huagongshe.com/de/reaction/441398

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktMethyl iodideHCID 6328—
EduktSodium hydrideHCID 24758—
Edukt8-chloro-1-[(aminooxy)methyl]6-phenyl-4H-s-triazolo[4,3-a][1,4]benzodiazepineHCID 12612426—
LösungsmittelDimethylformamideHCID 6228—
Produkt1H-1,4-BenzodiazepineHCID 148431—

Reaktionsschritte

A stirred solution of 8-chloro-1-[(aminooxy)methyl]6-phenyl-4H-s-triazolo[4,3-a][1,4]benzodiazepine (0.02 mole) in dry dimethylformamide (50 ml.) is cooled in an ice bath under nitrogen and treated successively with a 57% mineral oil suspension of sodium hydride (0.84 g,. 0.02 mole) and methyliodide (0.02 mole). The mixture is allowed to come slowly to ambient temperature and stand for 18 hours. It is then concentrated in vacuo. The residue is chromatographed on silica gel with methanol to give 8-chloro-1-[[(methylamino)oxy]methyl]6-phenyl-4H-s-triazolo]4,3-a][1,4]benzodiazepine.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS04039551
Quelldatensatzuspto-grants-1977_08
ORD IDord-d01ab87d9aa44073b1d7ec8d3cec7ccd
Quellennotizuspto-grants-1977_08