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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 472254Erstellt: 23. Oktober 2026

Diisopropylethylamine → 8-Bromo-(1,2,4)triazolo(1,5-a)pyridin-2-amine

https://huagongshe.com/de/reaction/472254

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktDiisopropylethylamineHCID 81531—
EduktHydroxyamine hydrochlorideHCID 443297—
EduktEthyl aminon-(3-bromopyridin-2-YL)methanethiocarbamateHCID 59199107—
LösungsmittelEthanolHCID 702—
LösungsmittelMethanolHCID 887—
Produkt8-Bromo-(1,2,4)triazolo(1,5-a)pyridin-2-amineHCID 46864069—

Reaktionsschritte

To a stirred suspension of hydroxylamine hydrochloride (17.4 g, 25.0 mmol) and N,N-diisopropylethylamine (26.0 mL, 14.9 mmol) in a mixture of methanol (70 mL) and ethanol (70 mL) was added N-(3-bromo-2-pyridinyl)-N′-carboethoxy-thiourea. The mixture was stirred for 2 hours at room temperature then heated to 60° C. for 18 hours. The suspension was cooled to room temperature, filtered and rinsed with methanol, water then methanol. 8-Bromo-[1,2,4]triazolo[1,5-a]pyridin-2-ylamine was isolated as an off-white solid (8.41 g, 70%). 1H NMR (400 MHz, (D3C)2SO, δ, ppm): 8.58 (d, J=6.4 Hz, 1H), 7.73 (d, J=7.6 Hz, 1H), 6.80 (t, J=7.0 Hz, 1H), 6.25 (s, 2H). MS=213, 215 (MH)+.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08633173B2
Quelldatensatzuspto-grants-2014_01
ORD IDord-0155977e33124d4ab5b61c2395a3ce80
Quellennotizuspto-grants-2014_01