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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 40205Erstellt: 23. Oktober 2026

Nitroethane → Tert-butyl (6-(3-methylisoxazol-5-yl)-[1,2,4]triazolo[4,3-b]pyridazin-3-yl)methylcarbamate

https://huagongshe.com/de/reaction/40205

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktNitroethaneHCID 6587—
EduktPhenyl isocyanateHCID 7672—
EduktTriethylamineHCID 8471—
Edukttert-Butyl (6-ethynyl-[1,2,4]triazolo[4,3-b]pyridazin-3-yl)methylcarbamateHCID 57691050—
LösungsmittelBenzeneHCID 241—
ProduktTert-butyl (6-(3-methylisoxazol-5-yl)-[1,2,4]triazolo[4,3-b]pyridazin-3-yl)methylcarbamateHCID 57691036—

Reaktionsbedingungen

Temperatur50 °C

Reaktionsschritte

To a solution of nitroethane (1.02 ml, 14.3 mmol) in benzene (50 mL) was added phenyl isocyanate (3.12 ml, 28.5 mmol). The mixture was stirred at 50° C. for twenty minutes followed by the addition of tert-butyl (6-ethynyl-[1,2,4]triazolo[4,3-b]pyridazin-3-yl)methylcarbamate (3.00 g, 11.0 mmol) and triethylamine (0.0765 ml, 0.549 mmol). The mixture was stirred at 50° C. for six hours then at room temperature overnight. The mixture was cooled to room temperature, filtered and the resulting brown precipitate was washed with additional benzene. The filtrate was concentrated to yield the product as a black solid. MS m/z=331.1 [M+1]+. Calc'd for C15H18N6O3: 330.1.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08524900B2
Quelldatensatzuspto-grants-2013_09
ORD IDord-d952825d729b4d20be4a45b727aa6332
Quellennotizuspto-grants-2013_09