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HRID 68652Erstellt: 24. Oktober 2026

Potassium Phosphate, Tribasic → 5-(4-(Isopropylsulfonyl)phenyl)pyrazin-2-amine

https://huagongshe.com/de/reaction/68652

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktPotassium Phosphate, TribasicHCID 62657—
Edukt2-Amino-5-bromopyrazineHCID 599539—
Edukt4-(Isopropylsulphonyl)benzeneboronic acidHCID 44119327—
KatalysatorHCID 178418851HCID 178418851—
LösungsmittelWaterHCID 962—
LösungsmittelAcetonitrileHCID 6342—
LösungsmittelEthyl AcetateHCID 8857—
Produkt5-(4-(Isopropylsulfonyl)phenyl)pyrazin-2-amineHCID 5808438280,7%

Reaktionsbedingungen

Temperatur60 °C

Reaktionsschritte

5-Bromopyrazin-2-amine (5 g, 28.74 mmol), (4-isopropylsulfonylphenyl) boronic acid (7.866 g, 34.49 mmol) and K3PO4 (12.20 g, 57.48 mmol) were combined in MeCN (100 mL)/Water (25 mL) and Pd[P(tBu)3]2 (734.4 mg, 1.437 mmol) was added. The reaction was heated at 60° C. for 1 hour. The reaction mixture was cooled to ambient temperature and diluted with EtOAc and water. The layers were separated and the aqueous layer extracted with EtOAc (×3). The combined organic layers were dried (MgSO4), filtered and concentrated in vacuo. The residue was triturated from DCM and isolated by filtration to give the sub-title compound as an orange solid (6.43 g, 76% Yield). 1H NMR (400.0 MHz, DMSO) δ 1.17 (d, 6H), 3.43 (sept, 1H), 6.86 (s, 2H), 7.87 (d, 2H), 8.00 (s, 1H), 8.20 (d, 2H) and 8.67 (s, 1H) ppm; MS (ES+) 278.2.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08822469B2
Quelldatensatzuspto-grants-2014_09
ORD IDord-61a69da484c1490a8b1889e647c37046
Quellennotizuspto-grants-2014_09