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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 271444Generated: October 31, 2026

Water → HCID 135465356, compound

https://huagongshe.com/reaction/271444

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantPotassium CarbonateHCID 11430—
Reactant5-(Chloromethyl)-2-(trifluoromethyl)pyridineHCID 2773810—
ReactantHCID 58772834HCID 58772834—
SolventDimethylformamideHCID 6228—
SolventEthyl AcetateHCID 8857—
ProductHCID 135465356HCID 135465356—

Reaction Conditions

Temperature50 °C

Reaction Steps

To a solution of 7,8-bis(4-chlorophenyl)-5-(1H-imidazol-1-yl)-[1,2,4]triazolo[4,3-c]pyrimidin-3(2H)-one (60 mg, 0.14 mmol) in DMF (0.5 mL) at room temperature under argon was added K2CO3 (25 mg, 0.18 mmol), followed by 5-(chloromethyl)-2-(trifluoromethyl)pyridine (28 mg, 0.14 mmol). The reaction mixture was stirred at 50° C. in a pre-heated oil bath for 30 min. After the reaction mixture was cooled to room temperature, water (5 mL) and EtOAc (5 mL) were added. The layers were separated. The organic layer was dried (MgSO4), filtered, and concentrated under reduced pressure. The crude product thus obtained was purified by preparative reverse phase HPLC (without TFA) to obtain 22.5 mg of the title compound as a white solid. HPLC/MS: retention time=3.871 min, [M+H]30 =532.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07452892B2
Source datasetuspto-grants-2008_11
ORD IDord-7b61fecdf9674a12a63e8b0ee5144f80
Source noteuspto-grants-2008_11