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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1465745Generated: October 30, 2026

Potassium Phosphate, Tribasic → tert-Butyl 4-(7-bromo-2-naphthyl)-3-oxopiperazine-1-carboxylate

https://huagongshe.com/reaction/1465745

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium Phosphate, TribasicHCID 62657—
Reactant1-N,2-N-dimethylcyclohexane-1,2-diamineHCID 551074—
Reactant2,7-DibromonaphthaleneHCID 625355—
ReactantTert-butyl 3-oxopiperazine-1-carboxylateHCID 3157178—
CatalystCopper(1+) iodide; Copper(I) iodide; Cuprous iodide; Cuprous iodide (CuI)HCID 24350—
Solvent1,4-DioxaneHCID 31275—
Producttert-Butyl 4-(7-bromo-2-naphthyl)-3-oxopiperazine-1-carboxylateHCID 131732665—

Reaction Conditions

Temperature150 °C

Reaction Steps

To a 20 mL microwave vial charged with 2,7-dibromonaphthalene (1.1 g, 3.8 mmol), tert-butyl 3-oxopiperazine-1-carboxylate (0.50 g, 2.5 mmol), and a stir bar was added copper (I) iodide (95 mg, 0.50 mmol), N,N′-dimethylcyclohexane-1,2-diamine (142 mg, 1.0 mmol), K3PO4 (1100 mg, 5.0 mmol), and dioxane (15 mL). The mixture was purged three times with nitrogen, and heated to 150° C. in a microwave reactor. The crude solution was diluted with EtOAc, adsorbed onto silica gel, and purified by silica gel chromatography (Hex:EtOAc). The solvent was removed to provide the title compound. LC-MS (IE, m/z): 405 [M+1]+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08999991B2
Source datasetuspto-grants-2015_04
ORD IDord-c0d3925e28e445d2a7e268e18f092f10
Source noteuspto-grants-2015_04