Reaktion #73022

Reaktionsgleichung

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

1-aminomethyl-1-cyclohexanol hydrochloride

triethylamine

→

1-{[(2-chloro-5,6-dimethyl-3-nitropyridin-4-yl)amino]methyl}cyclohexanol

Lösungsmittel

N,N-dimethylformamide

Reaktionsbedingungen

Aufarbeitung

1. 1
   TemperaturThe solution was heated to 35° C. for 3 d
2. 2
   SonstigeThe volatiles were removed under reduced pressure
3. 3
   Sonstigethe resulting oil was partitioned between dichloromethane (300 mL) and water (50 mL)
4. 4
   WaschenThe organic layer was washed with water (50 mL) and brine (30 mL)
5. 5
   Trocknendried over MgSO4
6. 6
   Filtrationfiltered
7. 7
   Einengenconcentrated under reduced pressure
8. 8
   Sonstigedried under vacuum

Vorschrift

A 500 mL round bottom flask was charged with 2,4-dichloro-5,6-dimethyl-3-nitropyridine (6.00 g, 27.1 mmol), 1-aminomethyl-1-cyclohexanol hydrochloride (4.94 g, 29.8 mmol), and N,N-dimethylformamide (200 mL). The solution was cooled to 0° C. and triethylamine (8.31 mL, 59.6 mmol) was added dropwise. The solution was heated to 35° C. for 3 d. The volatiles were removed under reduced pressure and the resulting oil was partitioned between dichloromethane (300 mL) and water (50 mL). The organic layer was washed with water (50 mL) and brine (30 mL), dried over MgSO4, filtered, concentrated under reduced pressure, and dried under vacuum to yield 1-{[(2-chloro-5,6-dimethyl-3-nitropyridin-4-yl)amino]methyl}cyclohexanol that was used without further manipulation in the next step.

Quelle