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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 553516Generated: October 30, 2026

Potassium Carbonate → 4-Fluoro-N-(2-{4-[2-(1H-indol-4-yl)-pyridin-3-yl]-piperazin-1-yl}-ethyl)-N-methyl-benzenesulfonamide hydrochloride

https://huagongshe.com/reaction/553516

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium CarbonateHCID 11430—
ReactantBoronic AcidHCID 61668—
Reactant1H-Indole-4-boronic acidHCID 2763173—
ReactantN-{2-[4-(2-Chloro-pyridin-3-yl)-piperazin-1-yl]-ethyl}-4-fluoro-N-methyl-benzenesulfonamideHCID 86640209—
CatalystHCID 178418397HCID 178418397—
Solvent1,2-DimethoxyethaneHCID 8071—
Product4-Fluoro-N-(2-{4-[2-(1H-indol-4-yl)-pyridin-3-yl]-piperazin-1-yl}-ethyl)-N-methyl-benzenesulfonamide hydrochlorideHCID 6736709315.1%

Reaction Conditions

Temperature80 °C

Reaction Steps

Dissolve N-{2-[4-(2-chloro-pyridin-3-yl)-piperazin-1-yl]-ethyl}-4-fluoro-N-methyl-benzenesulfonamide (0.160 g, 0.387 mmol) in DME (5 mL, previously degassed with nitrogen). Add 4-indole boronic acid (0.094 g, 0.581 mmol), 2N aqueous potassium carbonate (0.464 mL, 0.129 g, 0.930 mmol), and tetrakis(triphenylphosphine)palladium (0.022 g, 0.022 mmol). Stir the reaction mixture at 80° C. for 18 hr. Add fresh catalyst (0.015 g) and boronic acid (0.050 g). Stir an additional 8 hr. at 95° C. Cool to room temperature and concentrate to remove DME. Dilute with ethyl acetate and brine. Extract the aqueous layer with ethyl acetate. Combine the organic layers, dry over sodium sulfate, filter, and concentrate. Purify the resulting material by silica gel chromatography eluting with dichloromethane:methanol 94:6 to 90:10 to afford the title compound (0.031 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08048884B2
Source datasetuspto-grants-2011_11
ORD IDord-4bdadbb919334267b45f5d2714c15373
Source noteuspto-grants-2011_11