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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 271438Generated: October 25, 2026

Chloride → 5-(azetidin-1-yl)-7,8-bis(4-chlorophenyl)-2-((6-(trifluoromethyl)pyridin-3-yl)methyl)-[1,2,4]triazolo[4,3-c]pyrimidin-3(2H)-one

https://huagongshe.com/reaction/271438

Reaction equation

Participants

RoleNameHCIDCharge
ReactantChlorideHCID 312—
Reactant5-(Chloromethyl)-2-(trifluoromethyl)pyridineHCID 2773810—
Reactant1-(7,8-Bis(4-chlorophenyl)-2-ethyl-3-oxo-2,3-dihydro-[1,2,4]triazolo[4,3-c]pyrimidin-5-yl)-3-(ethylamino)azetidine-3-carboxamideHCID 15953098—
Reactant5-chloro-7,8-bis(4-chlorophenyl)-[1,2,4]triazolo[4,3-c]pyrimidin-3(2H)-oneHCID 58772840—
Product5-(azetidin-1-yl)-7,8-bis(4-chlorophenyl)-2-((6-(trifluoromethyl)pyridin-3-yl)methyl)-[1,2,4]triazolo[4,3-c]pyrimidin-3(2H)-oneHCID 15953244—

Reaction Steps

The title compound was prepared in two steps from 5-chloro-7,8-bis(4-chlorophenyl)-[1,2,4]triazolo[4,3-c]pyrimidin-3(2H)-one by nucleophilic displacement of chloride with the requisite amine, followed by alkylation with 5-(chloromethyl)-2-(trifluoromethyl)pyridine, in a manner analogous to that in which 1-(7,8-bis(4-chlorophenyl)-2-ethyl-3-oxo-2,3-dihydro-[1,2,4]triazolo[4,3-c]pyrimidin-5-yl)-3-(ethylamino)azetidine-3-carboxamide was prepared. HPLC/MS: retention time=4.483 min, [M+H]30 =571.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07452892B2
Source datasetuspto-grants-2008_11
ORD IDord-10c2946f61dd4726975f3fb31e632225
Source noteuspto-grants-2008_11