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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1414912Erstellt: 26. Oktober 2026

alpha-Hydroxytriazolam → 6-(o-chlorophenyl)-8-chloro-4H-s-triazolo[4,3-a][1,4] benzodiazepine-1-carboxaldehyde

https://huagongshe.com/reaction/1414912

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Eduktalpha-HydroxytriazolamHCID 1963—
KatalysatorHCID 178418406HCID 178418406—
LösungsmittelBenzeneHCID 241—
Produkt6-(o-chlorophenyl)-8-chloro-4H-s-triazolo[4,3-a][1,4] benzodiazepine-1-carboxaldehydeHCID 21486012—

Reaktionsschritte

A suspension of 1.3 g of 6-(o-chlorophenyl)-8-chloro-4H-s-triazolo[4,3-a][1,4]benzodiazepine-1-methanol and 3.4 g of manganese dioxide in 200 ml of benzene is refluxed for 2 hours. The reaction mixture is then filtered and the filtrate concentrated by evaporation. The resulting foam is dissolved in a little ethyl acetate and the solution chromatographed on ca. 60 g of silica gel (Merck, 0.063 - 0.2 mm particle size) with ethyl acetate as the eluant. Fractions each of ca. 80 ml are collected. The fractions 4-8 are combined, concentrated by evaporation, and the residue crystallised from an ethyl acetate/ether/petroleum ether mixture to obtain 6-(o-chlorophenyl)-8-chloro-4H-s-triazolo[4,3-a][1,4] benzodiazepine-1-carboxaldehyde, M.P. 182°-189°.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS04002764
Quelldatensatzuspto-grants-1977_01
ORD IDord-7dd22304101e42378d97781f697d154a
Quellennotizuspto-grants-1977_01