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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 61072Generated: October 25, 2026

3-Chloro-6-(trifluoromethyl)pyridazine → ((2S,3R)-3-Methyl-2-(((6-(trifluoromethyl)pyridazin-3-yl)amino)methyl)piperidin-1-yl)(5-methyl-2-(pyridin-2-yl)phenyl)methanone

https://huagongshe.com/reaction/61072

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3-Chloro-6-(trifluoromethyl)pyridazineHCID 28242526—
Reactant((2S,3R)-2-(Aminomethyl)-3-methylpiperidin-1-yl)(5-methyl-2-(pyridin-2-yl)phenyl)methanoneHCID 117727920—
Product((2S,3R)-3-Methyl-2-(((6-(trifluoromethyl)pyridazin-3-yl)amino)methyl)piperidin-1-yl)(5-methyl-2-(pyridin-2-yl)phenyl)methanoneHCID 117729258—

Reaction Steps

The title compound was prepared following the same general protocol as described for Example A1, using ((2S,3R)-2-(aminomethyl)-3-methylpiperidin-1-yl)(5-methyl-2-(pyridin-2-yl)phenyl)methanone and 3-chloro-6-trifluoromethylpyridazine. ESI-MS (m/z): 470 [M+1]+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09440982B2
Source datasetuspto-grants-2016_09
ORD IDord-5765310de30c444cb2a3bfe925e658c5
Source noteuspto-grants-2016_09