Reaktion #1095860

ord-9dd5b9e702244c0ca3e70902fa5c705e

Reaktionsgleichung

CCC#CCOc1ncnc(Cl)c1F
4-chloro-5-fluoro-6-(2-pentynyloxy)pyrimidine
CC1CCCNC1
3-methylpiperidine
CCC#CCOc1ncnc(N2CCCC(C)C2)c1F
5-fluoro-4-(3-methylpiperidino)-6-(2-pentynyloxy)pyrimidine
Ausbeute 89.0%

Reaktionsbedingungen

Detaillierte Bedingungen
See reaction.notes.procedure_details.

Vorschrift

0.2 g of 4-chloro-5-fluoro-6-(2-pentynyloxy)pyrimidine and 0.29 g of 3-methylpiperidine 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 5-fluoro-4-(3-methylpiperidino)-6-(2-pentynyloxy)pyrimidine (hereinafter, referred to as Compound (10)).

Quelle

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