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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1692137Generated: October 31, 2026

Tetrahydrofuran → HCID 24996068, compound

https://huagongshe.com/reaction/1692137

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTetrahydrofuranHCID 8028—
ReactantAmmonium HydroxideHCID 14923—
ReactantHCID 24996716HCID 24996716—
SolventWaterHCID 962—
SolventEthyl AcetateHCID 8857—
ProductHCID 24996068HCID 24996068—

Reaction Steps

To a vial containing ethyl 5-[2-(4-tert-butyl-benzenesulfonylamino)-5-chloro-4-fluoro-phenyl]-4-methyl-4H-[1,2,4]triazole-3-carboxylic acid ethyl ester (synthesized according to general procedure C, 100 mg, 0.202 mmol) was added THF (2 mL) and 28% NH4OH in water (2 mL), and the resultant solution was stirred at room temperature for 1 h. The reaction mixture was subsequently diluted with EtOAc (30 mL) and the organics were washed with water (2×10 mL), dried over Na2SO4, concentrated in vacuo, and purified by flash chromatography (50→100% gradient of EtOAc in hexanes). The pure fractions were collected and the solvent was removed. The isolated product was dissolved in MeCN/H2O and the solvent removed via lyophilization to afford the title compound as a white powder: MS (ES) M+H expected 466.0, found 466.0.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08153818B2
Source datasetuspto-grants-2012_04
ORD IDord-f4072de535154d4b9c7d3671e452074f
Source noteuspto-grants-2012_04