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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 79096Generated: October 29, 2026

Potassium Phosphate, Tribasic → HCID 24855059, compound

https://huagongshe.com/reaction/79096

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium Phosphate, TribasicHCID 62657—
Reactant2-(Piperidin-1-yl)phenolHCID 3262250—
Reactant2-bromo-N-(3-(aminosulfonyl)phenyl)benzamideHCID 26580511—
CatalystCopper(1+) iodide; Copper(I) iodide; Cuprous iodide; Cuprous iodide (CuI)HCID 24350—
SolventWaterHCID 962—
SolventDimethylformamideHCID 6228—
ProductHCID 24855059HCID 24855059—

Reaction Conditions

Temperature150 °C

Reaction Steps

A suspension of 2-bromo-N-(3-(aminosulfonyl)phenyl)benzamide (0.10 g, 0.28 mmol), 2-(piperidin-1-yl)phenol (74 mg, 0.28 mmol), K3PO4 (0.12 g, 0.56 mmol), and CuI (53 mg, 0.28 mmol) in DMF (1 mL) and water (20 μL) was sealed in a glass tube and heated in a microwave oven at 150° C. for 15 min. The reaction was filtered and purified by preparative reverse phase HPLC using 10%-99% CH3CN (0.035% TFA)/H2O (0.05% TFA) to give 2-(2-(piperidin-1-yl)phenoxy)-N-(3-(aminosulfonyl)phenyl)benzamide. LC/MS: m/z 452.0 (M+H)+ at 2.31 min (10%-99% CH3CN (0.035% TFA)/H2O (0.05% TFA)).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08841483B2
Source datasetuspto-grants-2014_09
ORD IDord-8ff2be434a974ceb848b4bf55ae14d5c
Source noteuspto-grants-2014_09