HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1747502Generated: November 1, 2026
Ethyl 4,4,4-trifluoroacetoacetate → HCID 178516597, compound
https://huagongshe.com/reaction/1747502
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Ethyl 4,4,4-trifluoroacetoacetate | HCID 67793 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Reactant | HCID 178507306 | HCID 178507306 | — |
| Solvent | Acetic Acid | HCID 176 | — |
| Product | HCID 178516597 | HCID 178516597 | 39.1% |
Reaction Steps
Ethyl trifluoroacetoacetate (1.28 g, 6.97 mmol) was added to a solution of 3-[1-(5-chloropyridin-2-yl)piperidin-4-yl]-1H-pyrazol-5-amine (0.484 g, 1.74 mmol) produced in Reference Example 20 in acetic acid (8 mL), and the mixture was stirred at 60° C. for 1.5 hours. A saturated sodium bicarbonate aqueous solution was added to the reaction solution, followed by extraction with ethyl acetate twice. 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=100/0-95/5 (gradient)] and further purified by silica gel column chromatography [elute: hexane/ethyl acetate=20/80-0/100 (gradient)] to obtain the title compound (0.283 g, yield: 39%).
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-f64b1a3ea22744bf9187e2ccc7b97b6c |
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| Source note | uspto-grants-2015_10 |
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