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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1265052Erstellt: 25. Oktober 2026

tert-butyl N-(4-aminobutyl)carbamate → Tert-butyl 4-(2-chloro-5,6-dimethyl-3-nitropyridin-4-yl)butylcarbamate

https://huagongshe.com/reaction/1265052

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Edukttert-butyl N-(4-aminobutyl)carbamateHCID 4351—
EduktDimethylformamideHCID 6228—
EduktTriethylamineHCID 8471—
Edukt2,4-Dichloro-5,6-dimethyl-3-nitropyridineHCID 12109123—
LösungsmittelEthyl AcetateHCID 8857—
ProduktTert-butyl 4-(2-chloro-5,6-dimethyl-3-nitropyridin-4-yl)butylcarbamateHCID 2197383079,8%

Reaktionsschritte

Tert-butyl 4-aminobutylcarbamate (60 g, 339 mmol) was slowly added to a mixture of 2,4-dichloro-5,6-dimethyl-3-nitropyridine (50 g, 226 mmol), anhydrous N,N-dimethylformamide (500 mL) and triethylamine (50 mL, 339 mmol). The reaction mixture was allowed to stir overnight and then it was concentrated under reduced pressure to provide an oil. The oil was dissolved in ethyl acetate and then washed with water. The organic layer was dried over magnesium sulfate and then concentrated under reduced pressure to provide a dark oil. This material was purified by column chromatography (silica gel eluting with 40/60 ethyl acetate/hexanes) to provide 64.5 g of tert-butyl 4-(2-chloro-5,6-dimethyl-3-nitropyridin-4-yl)butylcarbamate as a bright orange oil which solidified on standing.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS06545017B1
Quelldatensatzuspto-grants-2003_04
ORD IDord-47930171acaf48eaa51065f26c311c8e
Quellennotizuspto-grants-2003_04