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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1850754Generated: October 29, 2026

Triphenylphosphine → 1,1-Dimethylethyl 4-[(1R,2S)-2-[2-[4-(methylsulfonyl)phenoxy]ethyl]cyclopropyl]-1-piperidinecarboxylate

https://huagongshe.com/reaction/1850754

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriphenylphosphineHCID 11776—
Reactant4-(Methylsulfonyl)phenolHCID 123350—
ReactantDiisopropyl azodicarboxylateHCID 5363146—
ReactantHCID 66935605HCID 66935605—
SolventWaterHCID 962—
SolventTetrahydrofuranHCID 8028—
SolventEthyl AcetateHCID 8857—
Product1,1-Dimethylethyl 4-[(1R,2S)-2-[2-[4-(methylsulfonyl)phenoxy]ethyl]cyclopropyl]-1-piperidinecarboxylateHCID 70855958—

Reaction Conditions

Temperature0 °C

Reaction Steps

4-(methylsulfonyl)phenol (17 mg, 0.1 mmol), tert-butyl 4-[(1R,2S)-2-(2-hydroxyethyl)cyclopropyl)piperidine-1-carboxylate (27 mg, 0.1 mmol), and triphenylphosphine (70 mg, 0.21 mmol) were dissolved in tetrahydrofuran (1 mL) under an atmosphere of nitrogen and cooled at 0° C. DIAD (32 mg, 0.14 mmol) was added and the resulting mixture was warmed to RT and stirred overnight. The mixture was diluted with ethyl acetate (10 mL) and water (5 mL), and the layers were separated. The organic layer was washed with brine (2×10 mL), dried (Na2SO4), filtered, and concentrated under reduced pressure. The residue was purified by MS directed HPLC (30 minute, standard gradient 0-90% acetonitrile/water 0.1% formic acid buffer) and the fractions containing product combined. The solution was concentrated to dryness via GenoVac to afford the title compound. LC/MS (m/z): 424 (M+H)+. GPR119 Human EC50: 0.9 nM

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08957062B2
Source datasetuspto-grants-2015_02
ORD IDord-b9f416e08a384206b232ba7a720e5c30
Source noteuspto-grants-2015_02