Reacción #632020

Ecuación de reacción

1,4-diazabicyclo[3.2.2]nonane

2-chloro-5-nitro-pyrimidine

sodium bicarbonate

→

4-(5-Nitro-pyrimidin-2-yl)-1,4-diaza-bicyclo[3.2.2]nonane

Disolventes

dioxane

Condiciones de reacción

Tratamiento posterior

1. 1
   Extracciónfollowed by extraction with ethylacetate (3×20 ml)
2. 2
   OtroThe organic phase was dried
3. 3
   Otroevaporated
4. 4
   Otroa yellow powder was isolated

Procedimiento

A mixture of 1,4-diazabicyclo[3.2.2]nonane (0.87 g, 6.90 mmol), 2-chloro-5-nitro-pyrimidine (1.56 g, 6.27 mmol) and dioxane (75 ml) was stirred at room-temperature for 15 h. Aqueous sodium bicarbonate (20 ml, 10%) was added followed by extraction with ethylacetate (3×20 ml). The organic phase was dried and evaporated and a yellow powder was isolated. Yield 0.86 g (55%). Mp 135-139° C.

Fuente