Réaction #1095871

ord-f7d99bc22742489b940ba381b76ee424

Équation de réaction

CC#CCOc1cc(Cl)ncn1
4-chloro-6-(2-butynyloxy)pyrimidine
CCC1CCCCN1
2-ethylpiperidine
CC#CCOc1cc(N2CCCCC2CC)ncn1
4-(2-butynyloxy)-6-(2-ethylpiperidino)pyrimidine
Rendement 32.9%

Conditions de réaction

Conditions détaillées
See reaction.notes.procedure_details.

Mode opératoire

0.3 g of 4-chloro-6-(2-butynyloxy)pyrimidine and 0.56 g of 2-ethylpiperidine were mixed and left for 18 hours at 80° C. The reaction mixture was cooled to near room temperature and subjected to silica gel column chromatography to obtain 0.14 g of 4-(2-butynyloxy)-6-(2-ethylpiperidino)pyrimidine (hereinafter, referred to as Compound (22)).

Source

DOI: 10.6084/m9.figshare.5104873.v1Brevet: US07973028B2uspto-grants-2011_07