Reaction #1095874

ord-bc0c4512dfbe4d56a47b93b760af7ebb

Reaction equation

CCC#CCOc1cc(Cl)ncn1
4-chloro-6-(2-pentynyloxy)pyrimidine
FC(F)(F)C1CCCNC1
3-trifluoromethylpiperidine
CCC#CCOc1cc(N2CCCC(C(F)(F)F)C2)ncn1
6-(2-pentynyloxy)-4-(3-trifluoromethylpiperidino)pyrimidine
Yield 47.1%

Conditions

Detailed conditions
See reaction.notes.procedure_details.

Procedure

0.2 g of 4-chloro-6-(2-pentynyloxy)pyrimidine and 0.23 g of 3-trifluoromethylpiperidine were mixed and left for 10 hours at room temperature. The reaction mixture was subjected to silica gel column chromatography to obtain 0.15 g of 6-(2-pentynyloxy)-4-(3-trifluoromethylpiperidino)pyrimidine (hereinafter, referred to as Compound (25)).

Source

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