Reaktion #2305522

ord-610e693ba28f4aa7a1c5eec466af60e9

Reaktionsgleichung

Nc1cc(Br)cnc1N
5-bromo-2,3-diaminopyridine
CN(C)CCCOc1ccc(C=O)cc1
4-[3-(dimethylamino)-propoxy]benzaldehyde
→
CN(C)CCCOc1ccc(-c2nc3cc(Br)cnc3[nH]2)cc1
title compound
CN(C)CCCOc1ccc(-c2nc3cc(Br)cnc3[nH]2)cc1
N-{3-[4-(6-Bromo-3H-imidazo[4,5-b]pyridin-2-yl)phenoxy]propyl}-N,N-dimethylamine

Edukte

Nc1cc(Br)cnc1N
5-bromo-2,3-diaminopyridine
CN(C)CCCOc1ccc(C=O)cc1
4-[3-(dimethylamino)-propoxy]benzaldehyde

Reagenzien

Keine

Reaktionsbedingungen

Detaillierte Bedingungen
See reaction.notes.procedure_details.

Vorschrift

The title compound was prepared from 5-bromo-2,3-diaminopyridine (376 mg, 2 mmol) and 4-[3-(dimethylamino)-propoxy]benzaldehyde (420 mg, 2 mmol).

Quelle

DOI: 10.6084/m9.figshare.5104873.v1Patent: US07410966B2uspto-grants-2008_08