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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 328381Erstellt: 25. Oktober 2026

Methyl pyruvate → HCID 53751159, Verbindung

https://huagongshe.com/reaction/328381

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktMethyl pyruvateHCID 11748—
Edukt7-Chloro-2-hydrazinyl-5-phenyl-3H-1,4-benzodiazepineHCID 12390874—
LösungsmittelMethanolHCID 887—
ProduktHCID 53751159HCID 53751159—

Reaktionsschritte

A mixture of 5.7 g. (0.02 mole) of 7-chloro-2-hydrazino-5-phenyl-3H-1,4-benzodiazepine, 3 ml. (0.04 mole) of methyl pyruvate and 50 ml. of methanol is stirred, under nitrogen, for 17 hours at room temperature, by which time the solid has dissolved. Three ml. more methyl pyruvate is added and the solution is allowed to stand for 7 hours more. After filtration and evaporation in vacuo (50° C./0.5 mm.) a brown gum is obtained which is chromatographed on silica gel and eluted with 1% methanol in chloroform. Evaporation of the combined fractions containing the product (as indicated by thin layer chromatography) gives a gum which is crystallized from a mixture of chloroform and ether. A yield of 3.5 g. (67%) of 7-chloro-2-[[1-methoxycarbonyl)ethylidene]hydrazino]-5-phenyl-3H-1,4-benzodiazepine is obtained as nearly white crystals of melting point 156°-157° C. Melt solvate indicates the product contained 1.95% CHCl3 even after prolonged drying in vacuo.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS04017492
Quelldatensatzuspto-grants-1977_04
ORD IDord-e62459c7d01d41e2bcecb80f4214d39b
Quellennotizuspto-grants-1977_04