Reaktion #311065

ord-270801e1798747fb9e64df2e0f257301

Reaktionsgleichung

Cc1ccc(N)nc1
Cc1ccc(N)nc1
[C-]#[N+]C1CCCCC1
[C-]#[N+]C1CCCCC1
O=Cc1ccc(C(F)(F)F)cc1F
O=Cc1ccc(C(F)(F)F)cc
→
Cc1ccc2nc(-c3ccc(C(F)(F)F)cc3F)c(NC3CCCCC3)n2c1
Cc1ccc2nc(-c3ccc(C(F
Ausbeute 23.4%

Edukte

Cc1ccc(N)nc1
Cc1ccc(N)nc1
[C-]#[N+]C1CCCCC1
[C-]#[N+]C1CCCCC1
O=Cc1ccc(C(F)(F)F)cc1F
O=Cc1ccc(C(F)(F)F)cc1F

Reagenzien

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

Lösungsmittel

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

Reaktionsbedingungen

Temperatur
22°CELSIUS

Quelle

Imidazopyridines dataset