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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2250354Generated: November 2, 2026

Potassium Carbonate → HCID 58772593, compound

https://huagongshe.com/reaction/2250354

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium CarbonateHCID 11430—
Reactant5-(Chloromethyl)-2-(trifluoromethyl)pyridineHCID 2773810—
ReactantHCID 58772590HCID 58772590—
SolventWaterHCID 962—
SolventDimethylformamideHCID 6228—
ProductHCID 58772593HCID 5877259384%

Reaction Conditions

Temperature70 °C

Reaction Steps

A suspension of 6-chloro-7-(4-chlorophenyl)-[1,2,4]triazolo[4,3-b]pyridazin-3(2H)-one (843 mg, 3 mmol), 5-chloromethyl-2-(trifluoromethyl)pyridine (704 mg, 3.6 mmol) and solid K2CO3 (830 mg, 6 mmol) in anhydrous DMF (10 mL) was stirred at 70° C. for 20 min. Analysis by HPLC/MS indicated the reaction was complete. After cooling to room temperature, the reaction was diluted with water and extracted with EtOAc (40 mL×3). The combined EtOAc extracts were washed with saturated aqueous NaCl, dried (Na2SO4) and concentrated under reduced pressure. The crude product was purified by trituration with CH2Cl2-hexanes to afford 1.10 g (84%) of the title compound as a yellow solid. LC/MS (method A): retention time=3.50 min, (M+H)+=440.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07317012B2
Source datasetuspto-grants-2008_01
ORD IDord-028a993d0d124946bcc09fa15f1b87b5
Source noteuspto-grants-2008_01