Réaction #42844

ord-d6b2761139a1439abcd16946d8b3148b

Équation de réaction

Clc1cc(Cl)ncn1
4,6-dichloropyrimidine
CC1CNCC(C)C1
3,5-dimethylpiperidine
CC1CC(C)CN(c2cc(Cl)ncn2)C1
4-chloro-6-(3,5-dimethylpiperidino)pyrimidine
Rendement 66.0%

Conditions de réaction

Conditions détaillées
See reaction.notes.procedure_details.

Mode opératoire

0.3 g of 4,6-dichloropyrimidine and 0.34 g of 3,5-dimethylpiperidine (cis/trans diastereomer=about 3/1) were mixed and left for 5 hours at room temperature. The reaction mixture was subjected to silica gel column chromatography to obtain 0.3 g of 4-chloro-6-(3,5-dimethylpiperidino)pyrimidine. This compound had the cis/trans diastereomer originated two methyls on the pyperidine ring. The ratio of the cis/trans diastereomer was about 3.1/1.

Source

DOI: 10.6084/m9.figshare.5104873.v1Brevet: US07732448B2uspto-grants-2010_06