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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1472878Erstellt: 24. Oktober 2026

1-Benzyl-1H-pyrazole-4-boronic acid → 5-(1-Benzyl-1H-pyrazol-4-yl)-[1,2,4]triazolo[1,5-c]pyrimidin-2-ylamine

https://huagongshe.com/de/reaction/1472878

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Edukt1-Benzyl-1H-pyrazole-4-boronic acidHCID 3352881—
Edukt5-Methylsulfanyl-[1,2,4]triazolo[1,5-c]pyrimidin-2-ylamineHCID 59589529—
KatalysatorHCID 178418397HCID 178418397—
LösungsmittelTetrahydrofuranHCID 8028—
Produkt5-(1-Benzyl-1H-pyrazol-4-yl)-[1,2,4]triazolo[1,5-c]pyrimidin-2-ylamineHCID 59589583—

Reaktionsbedingungen

Temperatur130 °C

Reaktionsschritte

A microwave vial containing 5-methylsulfanyl-[1,2,4]triazolo[1,5-c]pyrimidin-2-ylamine (0.05 g, 0.276 mmol), 1-benzyl-1H-pyrazole-4-boronic acid (123 mg, 0.607 mmol), copper(1)thiophene carboxylate (116 mg, 0.607 mmol) and tetrakis(triphenylphosphine)palladium (33 mg, 0.028 mmol) in THF (1.2 mL) was heated under microwave irradiation (130° C., 15 min). The reaction mixture was filtered through celite and the cake washed with dichloromethane. The filtrate was washed with water followed by brine, dried over magnesium sulfate and concentrated under vacuum. Trituration with diethyl ether provided a yellow solid that did not require further purification. Yield: 0.05 g, 63%; LCMS method: 2, RT: 3.18 min, MI: 292 [M+1].

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS09012633B2
Quelldatensatzuspto-grants-2015_04
ORD IDord-6e160dad9d544c888671cea1d32f8f85
Quellennotizuspto-grants-2015_04