4-Bromo-2-fluorobenzoyl chloride → (4-Bromo-2-fluorophenyl) [4-(3,5,6-trimethylpyridin-2-yl)piperazin-1-yl]methanone

HRID 2411259Notizen

Reaktionsgleichung

Reaktionsgleichung von HRID 2411259
[Br:1][C:2]1[CH:10]=[CH:9][C:5]([C:6](Cl)=[O:7])=[C:4]([F:11])[CH:3]=1.Cl.[CH3:13][C:14]1[C:15]([N:22]2[CH2:27][CH2:26][NH:25][CH2:24][CH2:23]2)=[N:16][C:17]([CH3:21])=[C:18]([CH3:20])[CH:19]=1>>[Br:1][C:2]1[CH:10]=[CH:9][C:5]([C:6]([N:25]2[CH2:26][CH2:27][N:22]([C:15]3[C:14]([CH3:13])=[CH:19][C:18]([CH3:20])=[C:17]([CH3:21])[N:16]=3)[CH2:23][CH2:24]2)=[O:7])=[C:4]([F:11])[CH:3]=1

Komponenten

3

Edukt 2

HCID 27340264-Bromo-2-fluorobenzoyl chlorideHCID 673810521-(3,5,6-Trimethylpyridin-2-yl)piperazine hydrochloride

Produkt 1

HCID 58484847(4-Bromo-2-fluorophenyl) [4-(3,5,6-trimethylpyridin-2-yl)piperazin-1-yl]methanoneAusbeute 59,5 %

Versuchsvorschrift

Using 4-bromo-2-fluorobenzoyl chloride (5 g) and 1-(3,5,6-trimethylpyridin-2-yl)piperazine hydrochloride (5 g) described in Preparation Example 91 and by the reaction and treatment in the same manner as in Preparation Example 108, the title compound (5 g) was obtained.

Aufarbeitung

  1. customdescribed in Preparation Example 91 and by the reaction and treatment in the same manner as in Preparation Example 108

Quellen und Nachweise

ORD-Eintrag
ord-ad0e3972d124424fad6ecec92825a17c
Quelldatensatz
uspto-grants-2014_08
Patentnummer
US08816079B2

Notizen zur Reaktion

Wird geladen…