Reacción #311339

ord-02a6cbee10dc4fdc9d25ed24ae6ea6f5

Ecuación de reacción

Cc1ccc(N)nc1
Cc1ccc(N)nc1
[C-]#[N+]C1CCCCC1
[C-]#[N+]C1CCCCC1
O=Cc1cc(Br)c2c(c1)CCO2
O=Cc1cc(Br)c2c(c1)CC
→
Cc1ccc2nc(-c3cc(Br)c4c(c3)CCO4)c(NC3CCCCC3)n2c1
Cc1ccc2nc(-c3cc(Br)c
Rendimiento 11.1%

Reactantes

Cc1ccc(N)nc1
Cc1ccc(N)nc1
[C-]#[N+]C1CCCCC1
[C-]#[N+]C1CCCCC1
O=Cc1cc(Br)c2c(c1)CCO2
O=Cc1cc(Br)c2c(c1)CCO2

Reactivos

O=C(O)C(F)(F)F
trifluoroacetic acid

Disolventes

CC(C)O
isopropylalcohol
CC(C)O
isopropyl alcohol

Condiciones de reacción

Temperatura
22°CELSIUS

Fuente

Imidazopyridines dataset