Reacción #311013

ord-5e06ad56a0b94a10b694f08b44eedc69

Ecuación de reacción

Cc1ccc(N)nc1
Cc1ccc(N)nc1
[C-]#[N+]C1CCCCC1
[C-]#[N+]C1CCCCC1
N#Cc1ccc(Cl)c(C=O)c1
N#Cc1ccc(Cl)c(C=O)c1
→
Cc1ccc2nc(-c3cc(C#N)ccc3Cl)c(NC3CCCCC3)n2c1
Cc1ccc2nc(-c3cc(C#N)
Rendimiento 0.4%

Reactantes

Cc1ccc(N)nc1
Cc1ccc(N)nc1
[C-]#[N+]C1CCCCC1
[C-]#[N+]C1CCCCC1
N#Cc1ccc(Cl)c(C=O)c1
N#Cc1ccc(Cl)c(C=O)c1

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