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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 11343Erstellt: 24. Oktober 2026

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

https://huagongshe.com/de/reaction/11343

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
PatentnummerUS07098221B2
Quelldatensatzuspto-grants-2006_08
ORD IDord-1c8094ffd6f24c0698475b5c9484c8e6
Quellennotizuspto-grants-2006_08