Reaktion #1095900

ord-2a53cadc722a41a7be52f9801ad85197

Reaktionsgleichung

CCC=CCOc1cc(Cl)ncn1
4-chloro-6-(2-pentenyloxy)pyrimidine
C1=CCNCC1
1,2,3,6-tetrahydropyridine
CCC#CCOc1cc(N2C=CC=CC2)ncn1
1-(4-(2-pentynyloxy)pyrimidin-6-yl)pyridine
Ausbeute 63.1%

Reaktionsbedingungen

Detaillierte Bedingungen
See reaction.notes.procedure_details.

Vorschrift

0.3 g of 4-chloro-6-(2-pentenyloxy)pyrimidine and 0.25 g of 1,2,3,6-tetrahydropyridine were mixed and left for 3 hours at room temperature. The reaction mixture was subjected to silica gel column chromatography to obtain 0.23 g of 1-(4-(2-pentynyloxy)pyrimidin-6-yl)pyridine (hereinafter, referred to as Compound (55)).

Quelle

DOI: 10.6084/m9.figshare.5104873.v1Patent: US07973028B2uspto-grants-2011_07