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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 493427Generated: October 27, 2026

Triphenylphosphine → 6-(3-Piperidin-1-yl-propoxy)-quinoline-2-carboxylic acid ethyl ester

https://huagongshe.com/reaction/493427

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriphenylphosphineHCID 11776—
ReactantPiperidine-1-propanolHCID 66032—
ReactantEthyl 6-hydroxyquinoline-2-carboxylateHCID 57681568—
SolventTolueneHCID 1140—
SolventTetrahydrofuranHCID 8028—
Product6-(3-Piperidin-1-yl-propoxy)-quinoline-2-carboxylic acid ethyl esterHCID 57681571—

Reaction Conditions

Temperature35 °C

Reaction Steps

A mixture of 0.400 g (0.002 mol) of 6-hydroxy-quinoline-2-carboxylic acid ethyl ester, 0.966 g (0.004 mmol) of triphenylphospine (Fluka), 0.396 g (0.003 mmol) of 3-piperidin-1-yl-propan-1-ol and 0.68 ml (0.004 mmol) of di-tert.-butyl azadicarboxylate 40% in toluene in 40 ml THF was stirred for a prolonged period of time at 35° C. The mixture was filtered through a pad of silica and washed with 30 ml THF. The mixture was evaporated to dryness and purified on silica eluting with a gradient of DCM/MeOH/NH4OH from 97/3/0.5 to 90/10/0.5. The product fractions were evaporated and the residue was triturated with diethyl ether to yield after drying under vacuum 0.600 g (93%) of the title compound as white solid. MS (m/e): 343.3 (M+H)+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07534891B2
Source datasetuspto-grants-2009_05
ORD IDord-b00283c4652847368c5c1aa4a71f9cdd
Source noteuspto-grants-2009_05