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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1715514Generated: November 1, 2026

HCID 67482917, compound → HCID 67482779, compound

https://huagongshe.com/reaction/1715514

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHCID 67482917HCID 67482917—
ReactantHCID 86602022HCID 86602022—
SolventAcetonitrileHCID 6342—
ProductHCID 67482779HCID 67482779—

Reaction Steps

Ethyl 3-[2-fluoro-5-(trifluoromethyl)phenyl]-3-oxopropanoate (3 g, 9.7 mmol) and {(1S)-1-[4-(ethoxycarbonyl)phenyl]ethyl}hydrazinium trifluoroacetate (2.64 g, 8.2 mmol) were heated in dry acetonitrile (150 ml) to 85° C. for 8 hr. Solvent was evaporated and the residue purified by flash column chromatograph (SiO2, 25% ethyl acetate in hexanes) to give ethyl 4-((1S)-1-{3-[2-fluoro-5-(trifluoromethyl)phenyl]-5-oxo-4,5-dihydro-1H-pyrazol-1-yl}ethyl)benzoate as a white solid. NMR (500 MHz, CDCl3) δ: 1.38 (t, J=7.1, 3H); 1.82 (d, 7.2 Hz, 3H); 3.81 (dd, J=3 Hz, 23.9 Hz, 1H); 3.87 (dd, J=3 Hz, 23.9 Hz, 1H); 4.36 (q, J=7.1 Hz, 2H); 5.60 (q, J=7.2 Hz, 1H); 7.25 (t, J=9.5 Hz, 1H); 7.51 (d, J=8.4 Hz, 2H): 7.66 (br, 1H); 8.03 (d, J=8.4 Hz, 2H); 8.25 (dd, J=1.8 Hz, 6.4 Hz, 1H). MS C21H18F4N2O3

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07799818B2
Source datasetuspto-grants-2010_09
ORD IDord-4f060831caaa4a0b99e99ba8aa967380
Source noteuspto-grants-2010_09