Reaktion #311144

ord-aaa3a87a798b40f3b28138b5cea46a65

Reaktionsgleichung

Cc1ccc(N)nc1
Cc1ccc(N)nc1
[C-]#[N+]C1CCCCC1
[C-]#[N+]C1CCCCC1
O=CCc1ccc(Br)cc1
O=CCc1ccc(Br)cc1
→
Cc1ccc2nc(Cc3ccc(Br)cc3)c(NC3CCCCC3)n2c1
Cc1ccc2nc(Cc3ccc(Br)
Ausbeute 2.9%

Edukte

Cc1ccc(N)nc1
Cc1ccc(N)nc1
[C-]#[N+]C1CCCCC1
[C-]#[N+]C1CCCCC1
O=CCc1ccc(Br)cc1
O=CCc1ccc(Br)cc1

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