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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 392462Generated: October 31, 2026

Sodium Carbonate → HCID 23521687, compound

https://huagongshe.com/reaction/392462

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium CarbonateHCID 10340—
Reactant4-Cyanophenylboronic acidHCID 2734326—
ReactantHCID 23521705HCID 23521705—
CatalystHCID 178418397HCID 178418397—
Solvent1,4-DioxaneHCID 31275—
ProductHCID 23521687HCID 23521687—

Reaction Steps

A solution of N-(3-iodo-4-methylphenyl)-N-(ethylsulfonyl)pyrid-3-ylmethylamine (103 mg,0.247 mmol) and 4-cyanophenylboronic acid (55 mg, 0.371 mmol) in 4 ml of 1,4-dioxane stirring under nitrogen was treated with 2M sodium carbonate (0.37 mL, 0.741 mmol) and tetrakis(triphenylphosphine)palladium(0) (12.6 mg, 0.011 mmol). This was refluxed for three hours and then allowed to stir at room temperature for 16 hours. The reaction had not completed after this time so the reaction was treated with an additional 5.7 mg(0.005 mmol) of tetrakis(triphenylphosphine)palladium(0) and refluxed for two hours. The reaction was then cooled to room temperature and concentrated in vacuo. This was then dissolved in a minimal amount of dichloromethane and purified on a Chromatotron (200 omicron plate) with 3% methanol/dichloromethane to give a residue which was recrystallized using ether/hexanes to give the title compound. 1H NMR: 8.45-8.55 (d, 1H, J=4 Hz), 8.35-8.40 (s, 1H), 7.75-7.80 (d, 1H, J=12 Hz), 7.65-7.70 (d, 1H, J=12 Hz), 7.20-7.35 (m, 5H), 7.15-7.20 (m, 1H), 7.00-7.05 (s, 1H), 4.85-4.95 (s, 2H), 3.05-3.15 (q, 2H, J=10z), 2.15-2.20 (s, 3H), 1.40-1.50 (t, 3H, J=8 Hz); MS calcd. 391.5; MS (M+1)=392.1.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06800651B2
Source datasetuspto-grants-2004_10
ORD IDord-7d70624d0c3143a78fcc312e02c32c93
Source noteuspto-grants-2004_10