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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1783987Erstellt: 25. Oktober 2026

4-Iodoaniline → Tert-butyl 4-(4-aminophenyl)-3-oxopiperazine-1-carboxylate

https://huagongshe.com/reaction/1783987

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Edukt4-IodoanilineHCID 10893—
EduktPotassium CarbonateHCID 11430—
EduktTert-butyl 3-oxopiperazine-1-carboxylateHCID 3157178—
KatalysatorCopper(1+) iodide; Copper(I) iodide; Cuprous iodide; Cuprous iodide (CuI)HCID 24350—
Lösungsmittel1,4-DioxaneHCID 31275—
ProduktTert-butyl 4-(4-aminophenyl)-3-oxopiperazine-1-carboxylateHCID 5743753487%

Reaktionsbedingungen

Temperatur119 °C

Reaktionsschritte

A suspension of p-iodo-aniline (918 mg, 4.8 mmol), 3-oxo-piperazine-1-carboxylic acid tert-butyl ester (960 mg, 4.2 mmol) (1R,2R)-cyclohexane-1,2-diamine (0.05 mL, 0.42 mmol), copper (I) iodide (14.9 mg, 0.0042 mmol) and K2CO3 (1.19 g, 2.04 mmol) in dioxane (4 mL), is purged with nitrogen for 5 min in a reaction tube. The tube is sealed and the reaction mixture is heated at 119° C. for 15 hours. After cooling to room temperature, the reaction mixture is filtered through a silica cartridge washing with ethyl acetate (40 mL). The filtrate is concentrated in vacuo to afford the title compound as a brown liquid (1.06 g, 87%). LCMS: Rt 0.88 min (91%).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07501411B2
Quelldatensatzuspto-grants-2009_03
ORD IDord-d3d356812b1f43bf9733b56ece81d4c4
Quellennotizuspto-grants-2009_03