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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 277056Erstellt: 26. Oktober 2026

Benzaldehyde → 7-Bromo-2-phenyl-[1,2,4]triazolo[1,5-a]pyridin-5-ylamine

https://huagongshe.com/reaction/277056

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktBenzaldehydeHCID 240—
EduktPotassium HydroxideHCID 14797—
Edukt4-Bromo-2,6-diaminopyridineHCID 11435393—
EduktO-(2,4,6-Trimethylbenzenesulfonyl)hydroxylamineHCID 11830845—
LösungsmittelMethanolHCID 887—
Produkt7-Bromo-2-phenyl-[1,2,4]triazolo[1,5-a]pyridin-5-ylamineHCID 2262967339,3%

Reaktionsschritte

To a solution of 96 mg (0.51 mmol) 4-bromo-pyridine-2,6-diamine in 2.4 ml MeOH was added 121 mg (0.56 mmol) O-mesitylenesulfonylhydroxylamine (prepared from ethyl o-mesitylene-sulfonylacetohydroxamate and HClO4 (70%)) in 0.6 ml MeOH at −5° C. and after 15min 71 mg (0.56 mmol) benzaldehyde and stirred for 30 min. The addition of 4.8 ml 1N KOH was followed by extraction with ethylacetate, drying of the organic layer with Na2SO4, and removal of the volatile components. The residue was purified by column chromatography on silica eluting with ethylacetate and hexane (2:3). 58 mg(39%) of 7-bromo-2-phenyl-[1,2,4]triazolo[1,5-a]pyridin-5-ylamine were isolated, MS m/e (%): 290 (M++2, 44).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS06355653B1
Quelldatensatzuspto-grants-2002_03
ORD IDord-b9ea05ca0bc7405d99a5acc2a36743a9
Quellennotizuspto-grants-2002_03