Reaktion #11449

Reaktionsgleichung

tert-butyl 4-aminobutylcarbamate

2,4-dichloro-5,6-dimethyl-3-nitropyridine

triethylamine

→

tert-butyl 4-[(2-chloro-5,6-dimethyl-3-nitropyridin-4-yl)amino]butylcarbamate

Ausbeute 48.0%

Lösungsmittel

N,N-dimethylformamide

N,N-dimethylformamide

Reaktionsbedingungen

Aufarbeitung

1. 1
   Einengenconcentrated under reduced pressure
2. 2
   SonstigeThe residue was partitioned between water and ethyl acetate
3. 3
   SonstigeThe layers were separated
4. 4
   Extraktionthe aqueous layer was extracted with ethyl acetate
5. 5
   Waschenwashed with brine
6. 6
   Einengenconcentrated under reduced pressure
7. 7
   Sonstigeto provide a brown oily residue
8. 8
   SonstigeThis material was purified by flash chromatography (400 mL silica gel
9. 9
   Wascheneluting initially with 10% ethyl acetate in hexane
10. 10
    Temperaturincreasing the gradient to 15%

Vorschrift

A solution of tert-butyl 4-aminobutylcarbamate (8.52 g, 45.24 mmol) in N,N-dimethylformamide was added to a solution of 2,4-dichloro-5,6-dimethyl-3-nitropyridine (10.00 g, 45.24 mmol) and triethylamine (12.6 mL, 90.5 mmol) in N,N-dimethylformamide (320 mL). The reaction mixture was stirred overnight and then concentrated under reduced pressure. The residue was partitioned between water and ethyl acetate. The layers were separated and the aqueous layer was extracted with ethyl acetate. The organics were combined, washed with brine and then concentrated under reduced pressure to provide a brown oily residue. This material was purified by flash chromatography (400 mL silica gel, eluting initially with 10% ethyl acetate in hexane and then increasing the gradient to 15% and then to 25%) to provide 8.1 g of tert-butyl 4-[(2-chloro-5,6-dimethyl-3-nitropyridin-4-yl)amino]butylcarbamate as a yellow solid.

Quelle