Reaktion #167635

ord-b8d2b596116b447fb4343f3317b908e0

Reaktionsgleichung

Brc1cncc(N2CC3CC4CC2CN(C4)C3)c1
product
Brc1cncc(N2CC3CC4CC2CN(C4)C3)c1
4-(5-Bromopyridin-3-yl)-1,4-diazatricyclo[4.3.1.13,8]undecane
CC(=O)c1ccccc1B(O)O
2-acetylphenylboronic acid
→
CC(=O)c1ccccc1-c1cncc(N2CC3CC4CC2CN(C4)C3)c1
title compound
CC(=O)c1ccccc1-c1cncc(N2CC3CC4CC2CN(C4)C3)c1
1-{2-[5-(1,4-diazatricyclo[4.3.1.13,8]undec-4-yl)pyridin-3-yl]phenyl}ethanone

Edukte

Brc1cncc(N2CC3CC4CC2CN(C4)C3)c1
product
Brc1cncc(N2CC3CC4CC2CN(C4)C3)c1
4-(5-Bromopyridin-3-yl)-1,4-diazatricyclo[4.3.1.13,8]undecane
CC(=O)c1ccccc1B(O)O
2-acetylphenylboronic acid

Reagenzien

Keine

Reaktionsbedingungen

Detaillierte Bedingungen
See reaction.notes.procedure_details.

Vorschrift

The title compound was prepared from the product of Example 65A and 2-acetylphenylboronic acid according to General Method B: LC-MS Method D (ESI+) m/z 348.0 (M+H)+, retention time 1.26 minutes.

Quelle

DOI: 10.6084/m9.figshare.5104873.v1Patent: US08846661B2uspto-grants-2014_09