Reaktion #311344

ord-a8906feebbd44136904a199f6edc1db0

Reaktionsgleichung

Cc1ccc(N)nc1
Cc1ccc(N)nc1
[C-]#[N+]C1CCCCC1
[C-]#[N+]C1CCCCC1
O=Cc1cc2c(cc1Cl)OCO2
O=Cc1cc2c(cc1Cl)OCO2
→
Cc1ccc2nc(-c3cc4c(cc3Cl)OCO4)c(NC3CCCCC3)n2c1
Cc1ccc2nc(-c3cc4c(cc
Ausbeute 8.0%

Edukte

Cc1ccc(N)nc1
Cc1ccc(N)nc1
[C-]#[N+]C1CCCCC1
[C-]#[N+]C1CCCCC1
O=Cc1cc2c(cc1Cl)OCO2
O=Cc1cc2c(cc1Cl)OCO2

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