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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1623773Generated: October 31, 2026

Triphenylphosphine → 5-[(1-Methyl-4-piperidinyl)oxy]-2-[(phenylmethyl)oxy]-N-3-pyridinylbenzamide

https://huagongshe.com/reaction/1623773

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriphenylphosphineHCID 11776—
Reactant4-Piperidinol, 1-methyl-HCID 66048—
ReactantDiisopropyl azodicarboxylateHCID 5363146—
Reactant5-hydroxy-2-[(phenylmethyl)oxy]-N-3-pyridinylbenzamideHCID 51357514—
SolventTolueneHCID 1140—
Product5-[(1-Methyl-4-piperidinyl)oxy]-2-[(phenylmethyl)oxy]-N-3-pyridinylbenzamideHCID 51357516—

Reaction Conditions

Temperature115 °C

Reaction Steps

A solution of DIAD (0.30 ml, 1.56 mmol) in toluene (1 ml) was added dropwise to a solution of 5-hydroxy-2-[(phenylmethyl)oxy]-N-3-pyridinylbenzamide (may be prepared as described in Example 29; 200 mg, 0.624 mmol), 1-methyl-4-piperidinol (79 mg, 0.687 mmol) and Ph3P (409 mg, 1.561 mmol) in toluene under nitrogen at 0° C. The reaction mixture was stirred at 115° C. overnight. The mixture was then cooled and concentrated. The residue was added to water and extracted with ethyl acetate (3×60 ml). The organic phase was washed with saturated brine (30 ml), dried over sodium sulphate and evaporated in vacuo to give the crude product. The crude product was purified by Pre-TCL (DCM:methanol=8:1) to yield the title compound as a yellow solid. 36 mg.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08778939B2
Source datasetuspto-grants-2014_07
ORD IDord-5a81a0a6744744b895401e240d469f09
Source noteuspto-grants-2014_07