Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 625259Generated: October 30, 2026

Triphenylphosphine → 1-(2-(2-Nitro-5-(piperidin-1-yl)phenyl)pyridin-4-yl)-3-phenylpropan-1-one

https://huagongshe.com/reaction/625259

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriphenylphosphineHCID 11776—
ReactantHCID 66587487HCID 66587487—
Reactant1-(2-Bromopyridin-4-yl)-3-phenylpropan-1-oneHCID 86705936—
Catalystpalladium(II) acetateHCID 167845—
Solvent1,2-DimethoxyethaneHCID 8071—
SolventEthyl AcetateHCID 8857—
SolventSodium CarbonateHCID 10340—
Product1-(2-(2-Nitro-5-(piperidin-1-yl)phenyl)pyridin-4-yl)-3-phenylpropan-1-oneHCID 6751815781.5%

Reaction Steps

A solution of 200 mg of 1-(4-nitro-3-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl)piperidine 1.1e, 168 mg of 1-(2-bromopyridin-4-yl)-3-phenylpropan-1-one 5.1a, 12 mg of Pd(OAc)2, 58 mg of PPh3 in 1.25 mL of 2 N aqueous Na2CO3 solution and 3 mL of dimethoxyethane was refluxed for 4 h. The mixture was diluted with ethyl acetate and washed with water twice. The combined organic layer was dried over Na2SO4 and the solvent was evaporated. The residue was chromatographed on silica gel eluting with a gradient of 0% to 7% ethyl acetate in dichloromethane to give 196 mg of product.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09301951B2
Source datasetuspto-grants-2016_04
ORD IDord-71b72c41d58d4ed28fd3e96060d23a08
Source noteuspto-grants-2016_04