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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1384874Generated: October 27, 2026

Water → HCID 15125573, compound

https://huagongshe.com/reaction/1384874

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantPotassium;tri(butan-2-yl)boranuideHCID 4304157—
Reactant4-[4-[4-(4-Hydroxyphenyl)piperazin-1-yl]phenyl]-2-(3-oxobutan-2-yl)-1,2,4-triazol-3-oneHCID 15125565—
SolventDimethylformamideHCID 6228—
SolventTetrahydrofuranHCID 8028—
ProductHCID 15125573HCID 15125573—

Reaction Conditions

Temperature-10 °C

Reaction Steps

A mixture of (±)-2,4-dihydro-4-[4-[4-(4-hydroxyphenyl)-1-piperazinyl]phenyl]-2-(1-methyl-2-oxopropyl)-3H-1,2,4-triazol-3-one (0.06 mol) in DMF (500 ml) was cooled to −10° C. and then stirred under N2 flow. Potassium tri-sec-butylborohydride, 1 M solution in tetrahydrofuran (150 ml) was added dropwise. The mixture was allowed to warm to room temperature slowly and then poured out into water. The precipitate was filtered off, washed with CH3OH and crystallized from CH3OH. The precipitate was filtered off and dried. The residue was purified by HPLC over CHIRALPAC AD (eluent: ethanol). Two pure fractions were collected and their solvents were evaporated. Each residue was triturated in CH3OH. The precipitate was filtered off and dried, yielding 7.3 g [S-(R*,R )] -2,4-dihydro-2-(2-hydroxy-1 methylpropyl)-4-[4-[4-(4-hydroxyphenyl)-1-piperazinyl]phenyl]-3H-1,2,4-triazol-3-one. (interm. 1a) [α]20D=−10.81° (c=50.43 mg/5 ml DMF).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06262052B1
Source datasetuspto-grants-2001_07
ORD IDord-813bfa3c5fe64a2bbc559f87758fb5b4
Source noteuspto-grants-2001_07