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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2356391Generated: October 26, 2026

Potassium Carbonate → 4-(2-Ethyl-6-fluoro-3-{1-[3-(4-fluoro-phenylsulfanyl)-propyl]-piperidin-4-YL}-indol-1-YL)-benzoic acid ethyl ester

https://huagongshe.com/reaction/2356391

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium CarbonateHCID 11430—
ReactantN-methyl-2-pyrrolidoneHCID 13387—
ReactantEthyl 4-iodobenzoateHCID 142891—
Reactant2-Ethyl-6-fluoro-3-{1-[3-(4-fluoro-phenylsulfanyl)-propyl]-piperidin-4-yl}-1H-indoleHCID 57718837—
CatalystCopper iodideHCID 83717—
CatalystZinc OxideHCID 3007857—
SolventWaterHCID 962—
Product4-(2-Ethyl-6-fluoro-3-{1-[3-(4-fluoro-phenylsulfanyl)-propyl]-piperidin-4-YL}-indol-1-YL)-benzoic acid ethyl esterHCID 1195252526%

Reaction Conditions

Temperature160 °C

Reaction Steps

To a mixture of 2-ethyl-6-fluoro-3-{1-[3-(4-fluoro-phenylsulfanyl)-propyl]-piperidin-4-yl}-1H-indole (430 mg), p-iodobenzoic acid ethyl ester (716 mg), potassium carbonate (359 mg), copper iodide (52 mg) and zinc oxide (14 mg) in a reactor vial under argon is added NMP (3 ml) and the reaction heated by microwaves irradiation at 160° C. After 120 min, water is added and the suspension extracted with DCM. Preparative HPLC provides 150 mg pure product (26%) as a beige solid. R.t. 4.81 min.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07759365B2
Source datasetuspto-grants-2010_07
ORD IDord-539983f68fff4a7cb10bbbe8046a7874
Source noteuspto-grants-2010_07