HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 80716Generated: October 29, 2026
Trifluoroacetic acid → HCID 25145649, compound
https://huagongshe.com/reaction/80716
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Trifluoroacetic acid | HCID 6422 | — |
| Reactant | HCID 59406949 | HCID 59406949 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 25145649 | HCID 25145649 | 83% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08846676B2 |
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| Source dataset | uspto-grants-2014_09 |
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| ORD ID | ord-ad1d2d21c1d54d0abdfa09c68e1567ee |
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| Source note | uspto-grants-2014_09 |
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