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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 875945Erstellt: 24. Oktober 2026

N-Cyclohexylaniline → (5-Bromo-2-chloro-pyrimidin-4-yl)-cyclohexyl-phenyl-amine

https://huagongshe.com/de/reaction/875945

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktN-CyclohexylanilineHCID 74567—
Edukt5-Bromo-2,4-dichloropyrimidineHCID 289973—
LösungsmittelEthyl AcetateHCID 8857—
LösungsmittelN-methyl-2-pyrrolidoneHCID 13387—
Produkt(5-Bromo-2-chloro-pyrimidin-4-yl)-cyclohexyl-phenyl-amineHCID 5829958924%

Reaktionsbedingungen

Temperatur120 °C

Reaktionsschritte

5-Bromo-2,4-dichloropyrimidine (2.17 ml, 17.14 mmol) and cyclohexyl-phenyl-amine (2.0 g, 11.43 mmol) were dissolved in N-methylpyrrolidone (NMP) (25 ml), and this reaction was heated to 120° C. for 24 hours. The reaction was cooled to room temperature and diluted with ethyl acetate, washed with water and brine. The organic phase was dried using sodium sulfate and concentrated. Purification by flash chromatography (ethyl acetate/hexane) gave compound 37 as a yellow solid (855 mg, 24%). 1H NMR (500 MHz, DMSO-d6) δ ppm 8.27 (1 H, s), 7.41 (3 H, m), 7.21 (2 H, m), 4.62 (1 H, m), 1.93 (2 H, d, J=10 Hz), 1.75 (2 H, d, J=10 Hz), 1.58 (1 H, d, J=10 Hz), 1.34 (2 H, m), 1.15 (2 H, m), 0.91 (1 H, m).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08980903B2
Quelldatensatzuspto-grants-2015_03
ORD IDord-a85591db25ab4614b9c75c3381179b3d
Quellennotizuspto-grants-2015_03