Реакция #73022

Уравнение реакции

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

Растворители

N,N-dimethylformamide

Условия реакции

Обработка

1. 1
   ТемператураThe solution was heated to 35° C. for 3 d
2. 2
   ДругоеThe volatiles were removed under reduced pressure
3. 3
   Другоеthe resulting oil was partitioned between dichloromethane (300 mL) and water (50 mL)
4. 4
   ПромывкаThe organic layer was washed with water (50 mL) and brine (30 mL)
5. 5
   Сушкаdried over MgSO4
6. 6
   Фильтрацияfiltered
7. 7
   Концентрированиеconcentrated under reduced pressure
8. 8
   Другоеdried under vacuum

Методика

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.

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