Reaktion #1541785

ord-abbdf6bcb4f441e6b1ede55e639b4309

Reaktionsgleichung

O=[N+]([O-])c1cc(Cl)c(Cl)nc1Cl
3-nitro-2,5,6-trichloropyridine
Nc1ccc(CCO)cc1
4-aminophenylethyl alcohol
→
O=[N+]([O-])c1cc(Cl)c(Cl)nc1Nc1ccc(CCO)cc1
title compound
O=[N+]([O-])c1cc(Cl)c(Cl)nc1Nc1ccc(CCO)cc1
2-{4-[(5,6-Dichloro-3-nitro-2-pyridinyl)amino]phenyl}ethanol

Edukte

O=[N+]([O-])c1cc(Cl)c(Cl)nc1Cl
3-nitro-2,5,6-trichloropyridine
Nc1ccc(CCO)cc1
4-aminophenylethyl alcohol

Reagenzien

Keine

Reaktionsbedingungen

Detaillierte Bedingungen
See reaction.notes.procedure_details.

Vorschrift

The title compound was prepared according to the procedure described in step 1 of Example 34 from 3-nitro-2,5,6-trichloropyridine (Horn, U.; Mutterer, F.; Weis, C. D. Helv. Chim. Acta., 1976, 59,190. ) and 4-aminophenylethyl alcohol.

Quelle

DOI: 10.6084/m9.figshare.5104873.v1Patent: US07479564B2uspto-grants-2009_01