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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2290629Generated: October 30, 2026

Piperidine-2-methylamine → Flecainide

https://huagongshe.com/reaction/2290629

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPiperidine-2-methylamineHCID 90865—
ReactantBenzoyl chloride, 2,5-bis(2,2,2-trifluoroethoxy)-HCID 11427683—
ProductFlecainideHCID 3356—

Reaction Steps

In still another aspect of the invention, a method of preparing a 2,5-bis(2,2,2-trifluoroethoxy)-N-(2-piperidylmethyl)benzamide is provided which comprises the following steps. Hydroquinone is contacted with 2,2,2-trifluoroethyl trifluoromethanesulfonate under conditions to yield 1,4-bis(2,2,2-trifluoroethoxy)benzene. Then, in the presence of a Lewis acid catalyst, the 1,4-bis(2,2,2-trifluoroethoxy)benzene is treated with an acetylation agent under conditions to create 2,5-bis(2,2,2-trifluoroethoxy)acetophenone. The methyl moiety of the acetophenone function of the 2,5-bis(2,2,2-trifluoroethoxy)acetophenone is thereafter replaced using hypochlorite to yield 2,5-bis(2,2,2-trifluoroethoxy)benzoic acid. Subsequently, the 2,5-bis(2,2,2-trifluoroethoxy)benzoic acid is treated with an inorganic chloride to provide 2,5-bis(2,2,2-trifluoroethoxy)benzoic acid chloride. Finally, the resultant 2,5-bis(2,2,2-trifluoroethoxy)benzoic acid chloride is contacted with 2-aminomethylpiperidine, whereby there is formed 2,5-bis(2,2,2-trifluoroethoxy)-N-(2-piperidylmethyl)benzamide.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04617396
Source datasetuspto-grants-1986_10
ORD IDord-fdd01ea8d7e34bb497eec7bb15a636df
Source noteuspto-grants-1986_10