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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1027585Generated: October 30, 2026

1-Hydroxybenzotriazole → HCID 53241298, compound

https://huagongshe.com/reaction/1027585

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-HydroxybenzotriazoleHCID 75771—
ReactantO-(Benzotriazol-1-yl)-N,N,N',N'-tetramethyluronium tetrafluoroborateHCID 2733207—
Reactant4-(5-(3,5-Dichlorophenyl)-5-(tri fluoromethyl)-4,5-dihydroisoxazol-3-yl)-2-methylbenzoic acidHCID 23159811—
ReactantHCID 67246433HCID 67246433—
SolventAcetonitrileHCID 6342—
SolventTriethylamineHCID 8471—
ProductHCID 53241298HCID 53241298—

Reaction Steps

To a stirred solution of 4-[5-(3,5-dichloro-phenyl)-5-trifluoromethyl-4,5-dihydro-isoxazol-3-yl]-2-methyl-benzoic acid (1.75 g) (prepared according to WO 2009/080250) in acetonitrile (35 ml) and triethylamine (2.04 ml) were added under nitrogen atmosphere TBTU (1.61 g), AZA.HOBT (0.68 g) and C-(2-Benzyl-isoxazolidin-5-yl)-methylamine (Step B, 1.61 g) were added. The resulting solution was stirred at room temperature for 4 hours, then quenched by addition of aqueous saturated ammonium chloride solution. The mixture was then extracted with ethyl acetate, dried over sodium sulfate, filtered then concentrated in vacuo. The residue purified by column chromatography (ethyl acetate/cyclohexane 1:1) to afford the title compound as a white solid (60 mg, (mixture of diasteroisomers). LCMS (Method F) 2.20 min, M+H 636/638.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08735362B2
Source datasetuspto-grants-2014_05
ORD IDord-d98a7f04f5134df18a4da0f7db2ac514
Source noteuspto-grants-2014_05