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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 593171Erstellt: 24. Oktober 2026

Potassium Carbonate → 5-Bromo-1-methyl-3-(3-methylisothiazol-5-ylamino)pyrazin-2(1H)-one

https://huagongshe.com/de/reaction/593171

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktPotassium CarbonateHCID 11430—
Edukt3-Methylisothiazol-5-amineHCID 32307—
EduktBinap, (A+-)-HCID 634876—
Edukt3,5-Dibromo-1-methyl-1H-pyrazin-2-oneHCID 13062969—
Katalysatorpalladium(II) acetateHCID 167845—
Lösungsmittel1,4-DioxaneHCID 31275—
Produkt5-Bromo-1-methyl-3-(3-methylisothiazol-5-ylamino)pyrazin-2(1H)-oneHCID 8668460050%

Reaktionsbedingungen

Temperatur120 °C

Reaktionsschritte

A sealed tube equipped with a magnetic stirrer was charged with 3-methylisothiazol-5-amine (170 mg, 1.5 mmol), 3,5-dibromo-1-methylpyrazin-2(1H)-one (400 mg, 1.5 mmol), Pd(OAc)2 (84 mg, 0.375 mmol), BINAP (116 mg, 0.188 mmol), K2CO3 (450 mg, 4.5 mmol), and 1,4-dioxane (4 mL). After three cycles of vacuum/nitrogen flush, the mixture was heated at 120° C. in a sealed tube for 18 h. It was then cooled to room temperature and filtered. The filtrate was evaporated under reduced pressure. The residue was purified by silica-gel column chromatography eluting with dichloromethane/methanol (100:1 to 25:1) to afford 331a (220 mg, 50%) as a yellow solid. MS-ESI: [M+H]+ 301.0.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS09238655B2
Quelldatensatzuspto-grants-2016_01
ORD IDord-592e84d019cc4e5b96aa5a3cb6f87575
Quellennotizuspto-grants-2016_01