HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1754716Generated: October 28, 2026
Trifluoroacetic acid → 2-ethyl-5-(4-fluoro-benzylamino)-2H-pyrazole-3-carboxylic acid methyl ester
https://huagongshe.com/reaction/1754716
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Trifluoroacetic acid | HCID 6422 | — |
| Reactant | Triethylsilane | HCID 12052 | — |
| Reactant | 4-Fluorobenzaldehyde | HCID 68023 | — |
| Reactant | 5-amino-2-ethyl-2H-pyrazole-3-carboxylic acid methyl ester | HCID 57619416 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | 2-ethyl-5-(4-fluoro-benzylamino)-2H-pyrazole-3-carboxylic acid methyl ester | HCID 57619383 | — |
Reaction Steps
To 5-amino-2-ethyl-2H-pyrazole-3-carboxylic acid methyl ester (527, 1.00 g, 5.91 mmol) in acetonitrile (27.5 mL) were added 4-fluorobenzaldehyde (528, 0.660 mL, 6.26 mmol), triethylsilane (4.77 mL, 0.0298 mol) and trifluoroacetic acid (2.38 mL, 0.0310 mol). The reaction was stirred at 80° C. for 4 hours, then concentrated, poured into aqueous potassium carbonate, and extracted with ethyl acetate. The organic layer was dried over anhydrous sodium sulfate and filtered. The filtrate was concentrated and purified by silica gel column chromatography eluting with 20% to 100% ethyl acetate in hexane to give a white solid (529, 1.00 g, 61%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09169250B2 |
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| Source dataset | uspto-grants-2015_10 |
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| ORD ID | ord-48b459ee1f5646eb9b5121b72e3a7e9a |
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| Source note | uspto-grants-2015_10 |
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