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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 890532Generated: October 30, 2026

Sulfuric Acid → HCID 10275412, compound

https://huagongshe.com/reaction/890532

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSulfuric AcidHCID 1118—
ReactantEthyl AcetateHCID 8857—
ReactantHCID 22240395HCID 22240395—
SolventWaterHCID 962—
ProductHCID 10275412HCID 1027541241%

Reaction Steps

Part I. To 5-{[2-fluoro-4-(2-oxo-1(2H)-pyridinyl)phenyl]acetyl)-1-(4-methoxyphenyl)-1H-pyrazole-3-carbonitrile (75 mg, 0.175 mmol) was added concentrated aqueous dihydrogen sulfate (4.5 mL). After 2 h, the reaction was poured into ethyl acetate (50 mL) and water (50 mL), and the layers were separated. The organic layer was washed with saturated aqueous sodium chloride (50 mL), dried over sodium sulfate, and concentrated to dryness. The resulting residue was purified by radial chromatography (2% methyl alcohol in dichloromethane) to afford 5-{[2-fluoro-4-(2-oxo-1(2H)-pyridinyl)phenyl]acetyl}-1-(4-methoxyphenyl)-1H-pyrazole-3-carboxamide (32 mg, 41%) as a white solid upon lyopholization from 10% acetonitrile in water. LC/MS (ESI+): 448.2 (M+H)+. 1H NMR (CD3OD) δ 7.70 (s, 1H), 7.60 (m, 2H), 7.43 (t, 1H), 7.16–7.32 (m, 4H), 6.97 (d, 2H), 6.60 (d, 1H), 6.45 (t, 1H), 4.40 (s, 2H), 3.83 (s, 3H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06995172B2
Source datasetuspto-grants-2006_02
ORD IDord-4d2eff4cc1254c1d88a2ab6c72a0c6bf
Source noteuspto-grants-2006_02