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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1966455Generated: October 30, 2026

Potassium Phosphate, Tribasic → N-(2-(4-benzoylpiperazin-1-yl)-5-nitrophenyl)benzenamine

https://huagongshe.com/reaction/1966455

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium Phosphate, TribasicHCID 62657—
ReactantPhenylboronic AcidHCID 66827—
Reactant(4-(2-Amino-4-nitrophenyl)piperazin-1-yl)(phenyl)methanoneHCID 58425640—
CatalystCupric acetateHCID 8895—
SolventDichloromethaneHCID 6344—
ProductN-(2-(4-benzoylpiperazin-1-yl)-5-nitrophenyl)benzenamineHCID 4619922120%

Reaction Steps

A suspension of (4-(2-amino-4-nitrophenyl)piperazin-1-yl)(phenyl)methanone (0.4 g, 1.2 mmol), copper acetate (0.45 g, 2.5 mmol), potassium phosphate (0.26 g, 1.2 mmol), 18-C-6 (31 mg, 0.12 mmol), 4 Å molecular sieves (1.0 g) and phenylboronic acid and pyridine complex (1.4 g, 3.7 mmol) in 30 ml dry dichloromethane was stirred at room temperature overnight. The reaction was quenched with 20 ml water. The mixture was filtered and extracted with ethyl acetate (3×20 ml), followed by drying over anhydrous sodium sulfate. N-(2-(4-benzoylpiperazin-1-yl)-5-nitrophenyl)benzenamine (0.11 g, 20%) was obtained by flash column chromatograph (50% ethyl acetate in hexanes). 1H NMR (500 MHz, CDCl3) δ (ppm) 3.08 (s, br, 4H), 3.70 (s, br, 4H), 6.43 (s, 1H), 7.12-7.75 (m, 11H), 7.77 (d, J=2.4 Hz, 1H), 8.09 (s, 1H). 13C NMR (125 MHz, CDCl3): δ (ppm) 51.4, 108.9, 115.8, 120.2, 120.7, 123.8, 127.6, 128.5, 129.1, 130.3, 130.5, 135.8, 139.1, 141.1, 145.5, 145.9, 171.1.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08420640B2
Source datasetuspto-grants-2013_04
ORD IDord-19b63a587dd74962a329b34d4eda2834
Source noteuspto-grants-2013_04