HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1747501Generated: October 30, 2026
Ethyl 4,4,4-trifluoroacetoacetate → HCID 178516595, compound
https://huagongshe.com/reaction/1747501
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Ethyl 4,4,4-trifluoroacetoacetate | HCID 67793 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Reactant | HCID 178507305 | HCID 178507305 | — |
| Solvent | Acetic Acid | HCID 176 | — |
| Product | HCID 178516595 | HCID 178516595 | 48% |
Reaction Steps
Ethyl trifluoroacetoacetate (1.50 g, 8.15 mmol) was added to a solution of 3-{1-[5-(trifluoromethyl)pyridin-2-yl]piperidin-4-yl}-1H-pyrazol-5-amine (880 mg, 2.83 mmol) produced in Reference Example 10 in acetic acid (10 mL), and the mixture was stirred at 60° C. for 2 hours. A saturated sodium bicarbonate aqueous solution was added to the reaction solution, followed by extraction with ethyl acetate three times. The obtained organic layer was washed with brine and dried over anhydrous magnesium sulfate, and the solvent was distilled off under reduced pressure. The obtained residue was purified by silica gel column chromatography [NH-silica gel column, elute: ethyl acetate/methanol=100/0-96/4 (gradient)] and further purified by silica gel column chromatography [elute: hexane/ethyl acetate=60/40-0/100 (gradient)] to obtain the title compound (610 mg, yield: 48%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09150575B2 |
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| Source dataset | uspto-grants-2015_10 |
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| ORD ID | ord-50c842f5f2e14108a3848a44a5d76bd3 |
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| Source note | uspto-grants-2015_10 |
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