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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1850780Generated: November 2, 2026

Triphenylphosphine → 4-((1R,2S)-2-{2-[4-(2-azetidin-1-yl-2-oxoethyl)-2-fluorophenoxy]ethyl}cyclopropyl)-1-(3-isopropyl-1,2,4-oxadiazol-5-yl)piperidine

https://huagongshe.com/reaction/1850780

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriphenylphosphineHCID 11776—
ReactantDi-tert-butyl azodicarboxylateHCID 97268—
Reactant2-((1S,2R)-2-(1-(3-isopropyl-1,2,4-oxadiazol-5-yl)piperidin-4-yl)cyclopropyl)ethanolHCID 70818651—
Reactant1-(Azetidin-1-yl)-2-(3-fluoro-4-hydroxyphenyl)ethanoneHCID 70819132—
SolventDichloromethaneHCID 6344—
Product4-((1R,2S)-2-{2-[4-(2-azetidin-1-yl-2-oxoethyl)-2-fluorophenoxy]ethyl}cyclopropyl)-1-(3-isopropyl-1,2,4-oxadiazol-5-yl)piperidineHCID 70818506—

Reaction Steps

To a solution of 1-(azetidin-1-yl)-2-(3-fluoro-4-hydroxyphenyl)ethanone (65.0 mg, 0.236 mmol) in 5 ml anhydrous dichloromethane at RT was added a solution of 2-{(1S,2R)-2-[1-(3-isopropyl-1,2,4-oxadiazol-5-yl)piperidin-4-yl]cyclopropyl}ethanol (59.0 mg, 0.283 mmol), triphenylphosphine, polymer-bound (186 mg, 0.534 mmol), and di-tert-butyl azodicarboxylate (109 mg, 0.472 mmol). The reaction mixture as stirred at RT for 3 hours. The mixture was filtered by Celite and concentrated. The residue The reaction mixture was filtered and purified by reverse-phase HPLC (SunFire Prep C18 OBD 5 um 19×100 mm column; 35-100% acetonitrile in 0.1% formic acid in water gradient), to give the title compound. LC/MS (m/z) 471.3 (M+H)+. Human EC50: 5.3 nM

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08957062B2
Source datasetuspto-grants-2015_02
ORD IDord-51c681f01f1b463180fa7652bea59005
Source noteuspto-grants-2015_02