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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1510503Erstellt: 25. Oktober 2026

O-(2-(Vinyloxy)ethyl)hydroxylamine → 2-(4-Bromo-2-fluorophenylamino)-1-methyl-6-oxo-1,6-dihydropyridine-3-carboxylic acid (2-hydroxyethoxy)-amide

https://huagongshe.com/reaction/1510503

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktO-(2-(Vinyloxy)ethyl)hydroxylamineHCID 21867017—
Edukt2-(4-Bromo-2-fluorophenylamino)-1-methyl-6-oxo-1,6-dihydropyridine-3-carboxylic acidHCID 57636936—
Edukt2-(4-Bromo-2-fluorophenylamino)-1-methyl-6-oxo-1,6-dihydropyridine-3-carboxylic acid (2-vinyloxyethoxy)-amideHCID 86672323—
Produkt2-(4-Bromo-2-fluorophenylamino)-1-methyl-6-oxo-1,6-dihydropyridine-3-carboxylic acid (2-hydroxyethoxy)-amideHCID 1123496860%

Reaktionsschritte

Preparation of 2-(4-bromo-2-fluorophenylamino)-1-methyl-6-oxo-1,6-dihydropyridine-3-carboxylic acid (2-vinyloxyethoxy)-amide: 2-(4-Bromo-2-fluorophenylamino)-1-methyl-6-oxo-1,6-dihydropyridine-3-carboxylic acid (0.020 g, 0.059 mmol) was coupled as described previously in Example 154 using O-(2-vinyloxy-ethyl)-hydroxylamine to yield 0.015 g (60%) pure desired product as a yellow solid.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08211920B2
Quelldatensatzuspto-grants-2012_07
ORD IDord-2e249bf7a87545a88530f0c518a8b07e
Quellennotizuspto-grants-2012_07