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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1864181Generated: October 26, 2026

Toluene → 4-[8-(4-Methylsulfanyl-phenyl)quinolin-4-yloxy]-piperidine-1-carboxylic acid isopropyl ester

https://huagongshe.com/reaction/1864181

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTolueneHCID 1140—
ReactantSodium CarbonateHCID 10340—
Reactant4-(Methylthio)phenylboronic acidHCID 2733959—
Reactant4-(8-Chloro-quinolin-4-yloxy)-piperidine-1-carboxylic acid isopropyl esterHCID 57496380—
CatalystHCID 178418397HCID 178418397—
SolventEthyl AcetateHCID 8857—
Product4-[8-(4-Methylsulfanyl-phenyl)quinolin-4-yloxy]-piperidine-1-carboxylic acid isopropyl esterHCID 11407941—

Reaction Steps

In a 25 mL round-bottomed flask equipped with a reflux condenser and N2 inlet septum was placed a stir bar, 4-(8-chloro-quinolin-4-yloxy)-piperidine-1-carboxylic acid isopropyl ester (198 mg, 0.57 mmol), 4-methylthiophenylboronic acid (287 mg, 1.7 mmol), tetrakis(triphenylphosphine)palladium (98 mg, 0.085 mmol), 2M sodium carbonate (0.6 mL) and toluene (4 mL). The mixture was refluxed 36 h under N2. The resulting mixture was diluted with ethyl acetate and extracted with H2O. The organic extract was dried and concentrated to give the crude product. The crude product was purified by column chromatography to using 50% EtOAc/Hexane and preparative HPLC to give the desired product. 1H NMR (CDCl3, 400MHz) δ 1.27 (d, 6H), 2.04 (m, 2H), 2.17 (m, 2H), 2.55 (s, 3H), 3.59 (m, 2H), 3.83 (m, 2H), 4.97 (m, 1H), 5.09 (m, 1H), 7.14 (s, 1H), 7.41 (m, 4H), 7.81 (t, 1H), 7.90 (d, 1H), 8.38 (d, 1H), 9.11 (s, 1H). Exact mass calculated for C25H28N2O3S 436.18, found 437.2 (MH+).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07625906B2
Source datasetuspto-grants-2009_12
ORD IDord-d7372beef36a4a96bc7d9061cd4615c8
Source noteuspto-grants-2009_12