Reaktion #1095899

ord-18f091cc1a8247c7bcf05d629f555710

Reaktionsgleichung

CC#CCOc1cc(Cl)ncn1
4-chloro-6-(2-butynyloxy)pyrimidine
C1=CCNCC1
1,2,3,6-tetrahydropyridine
CC#CCOc1cc(N2CC=CCC2)ncn1
1-(6-(2-butynyloxy)pyrimidin-4-yl)-1,2,3,6-tetrahydropyridine
Ausbeute 100.9%

Reaktionsbedingungen

Detaillierte Bedingungen
See reaction.notes.procedure_details.

Vorschrift

0.3 g of 4-chloro-6-(2-butynyloxy)pyrimidine and 0.41 g of 1,2,3,6-tetrahydropyridine were mixed and left for 2 hours at room temperature. The reaction mixture was subjected to silica gel column chromatography to obtain 0.38 g of 1-(6-(2-butynyloxy)pyrimidin-4-yl)-1,2,3,6-tetrahydropyridine (hereinafter, referred to as Compound (54)).

Quelle

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