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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 324244Generated: October 30, 2026

Water → HCID 54142543, compound

https://huagongshe.com/reaction/324244

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantEthyl AcetateHCID 8857—
ReactantSodium HydroxideHCID 14798—
ReactantHCID 54013279HCID 54013279—
SolventEthanolHCID 702—
SolventTetrahydrofuranHCID 8028—
ProductHCID 54142543HCID 54142543—

Reaction Steps

To a solution of 46.5 mg (0.098 mmol) ethyl 2-fluoro-4-[[(5,6-dihydro-5,5-dimethyl-8-(4-methylphenyl)-2-naphthalenyl)thiocarbonyl]amino]-benzoate (Compound 62) in 1.0 ml EtOH and 1.0 ml of THF was added 55 mg NaOH (1.4 mmol) and 1.0 ml of H2O. After stirring at room temperature for overnight EtOAc was added, and the reaction quenched by the addition of 10% HCl. Extraction with EtOAc was followed by washing of the combined organic layers with H2O, saturated aqueous NaCl, and drying over MgSO4. Removal of the solvent under reduced pressure provided a solid which after crystallization from CH3CN afforded the title compound as a pale-yellow solid. 1H NMR (d6-acetone): δ 11.05 (1H, s), 8.02 (1H, m), 7.99 (1H, t, J=8.3 Hz), 7.75 (1H, m), 7.69 (1H, dd, J=2.0, 6.1 Hz), 7.52 (1H, s), 7.46 (1H, d, J=8.1 Hz), 7.21 (4H, m), 6.04 (1H, t, J=4.8 Hz), 2.37 (2H, d, J=4.8 Hz), 2.33 (3H, s), 1.36 (6H, s).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06218128B1
Source datasetuspto-grants-2001_04
ORD IDord-a53690846955496ebc5b6964dffb0a2e
Source noteuspto-grants-2001_04