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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2223709Generated: October 25, 2026

4-Benzyl-4-piperidinol → Palosuran

https://huagongshe.com/reaction/2223709

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-Benzyl-4-piperidinolHCID 98152—
ReactantSodium BicarbonateHCID 516892—
Reactant1-(2-Chloroethyl)-3-(2-methylquinolin-4-yl)ureaHCID 2344366—
SolventDichloromethaneHCID 6344—
SolventTetrahydrofuranHCID 8028—
ProductPalosuranHCID 10173280—

Reaction Conditions

Temperature45 °C

Reaction Steps

To a solution of 4-hydroxy-4-benzyl-piperidine (380.6 mg, 2 mmol) in dry THF (10 mL) is added 1-(2-chloro-ethyl)-3-(2-methyl-quinolin-4-yl)-urea (263.7 mg, 1 mmol) and solid NaHCO3 (672 mg, 8 mmol). The reaction mixture is stirred at 45° C. for 6 days. The reaction mixture is diluted with CH2Cl2 (100 mL) and washed with sat. Na2CO3 (2×30 mL). The aqueous phase is re-extracted with CH2Cl2 (2×25 mL), the combined organic phases are washed with brine (20 mL), dried (Na2SO4), filtered and evaporated. The residue is purified by preparative HPLC to provide the title compound.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07375227B2
Source datasetuspto-grants-2008_05
ORD IDord-a7135f3aee1c4ce9b0a672eb0e1b3c3f
Source noteuspto-grants-2008_05