1-[3-[3,5-bis(trifluoromethyl)phenyl]prop-2-ynyl]-4-tert-butyl-piperid ine
Piperidine, 1-[3-[3,5-bis(trifluoromethyl)phenyl]-2-propyn-1-yl]-4-(1,1-dimethylethyl)-
The industrial scale manufacturing of flupropadine is not described in open literature, but its structure and the limited synthetic information available indicate that commercial production followed a straightforward modular assembly of three components: (1) synthesis of the tert butylpiperidine ring, (2) preparation of the bis(trifluoromethyl)phenyl substituted propargyl intermediate, and (3) N alkylation of the piperidine with the propargyl side chain to form the final tertiary amine. A key step involved coupling the substituted propargyl fragment with the tert butylpiperidine core, consistent with standard late 20th century amine alkylation processes used for lipophilic rodenticides.
