HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1437288Generated: November 1, 2026
Trifluoroacetic acid → HCID 10451352, compound
https://huagongshe.com/reaction/1437288
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Trifluoroacetic acid | HCID 6422 | — |
| Reactant | HCID 57940651 | HCID 57940651 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 10451352 | HCID 10451352 | — |
Reaction Steps
At room temperature, trifluoroacetic acid (2.4 mL) was added to a solution of the above-mentioned 1-[1-(6-methoxy-3-pyridyl)-5-phenylpyrazole-3-carbonyl]piperazine-4-carboxylic acid tert-butyl ester (0.639 g) in methylene chloride (15 mL), followed by stirring of the mixture for 0.7 hours. The reaction solvent was removed under reduced pressure, and the residue was partitioned between chloroform and saturated aqueous sodium hydrogencarbonate. The aqueous layer was extracted with chloroform. The organic layers were combined and washed with saturated brine, followed by drying over sodium sulfate anhydrate. After filtration, the solvent was removed under reduced pressure. The residue was purified through silica gel column chromatography (chloroform-methanol), to thereby give the title compound as an oily product (0.446 g, 89%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07622471B2 |
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| Source dataset | uspto-grants-2009_11 |
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| ORD ID | ord-f2c491db6333426080d2aaf346a6ab05 |
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| Source note | uspto-grants-2009_11 |
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