Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1803882Generated: November 1, 2026

Trifluoroacetic acid → HCID 25145649, compound

https://huagongshe.com/reaction/1803882

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrifluoroacetic acidHCID 6422—
ReactantHCID 59406949HCID 59406949—
SolventDichloromethaneHCID 6344—
ProductHCID 25145649HCID 2514564983%

Reaction Steps

To a solution of 0.43 g (0.86 mmol) of tert-butyl 4-[2-(4-fluorophenyl)-7,8-dimethyl-3-pyrid-4-ylimidazo[1,2-b]pyridazin-6-yl]piperazine-1-carboxylate in 5 mL of dichloromethane at 0° C. is added dropwise 0.64 mL (8.6 mmol) of trifluoroacetic acid. After stirring for 4 hours at room temperature, a further 0.64 mL (8.6 mmol) of trifluoroacetic acid is added and the reaction mixture is left for 18 hours. The solvent is then removed under reduced pressure and the residue is taken up in water. The resulting aqueous phase is washed with ether and then basified by addition of aqueous sodium hydrogen carbonate solution. The product is extracted with dichloromethane, the organic phase is dried over sodium sulfate and filtered, and the solvent is evaporated off to give 0.285 g of a white powder.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08354405B2
Source datasetuspto-grants-2013_01
ORD IDord-5e0d419ddccc46d2844cd030176d8df1
Source noteuspto-grants-2013_01