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
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
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| Edukt | 1-Benzyl-1H-pyrazole-4-boronic acid | HCID 3352881 | — |
| Edukt | 5-Methylsulfanyl-[1,2,4]triazolo[1,5-c]pyrimidin-2-ylamine | HCID 59589529 | — |
| Katalysator | HCID 178418397 | HCID 178418397 | — |
| Lösungsmittel | Tetrahydrofuran | HCID 8028 | — |
| Produkt | 5-(1-Benzyl-1H-pyrazol-4-yl)-[1,2,4]triazolo[1,5-c]pyrimidin-2-ylamine | HCID 59589583 | — |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US09012633B2 |
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| Quelldatensatz | uspto-grants-2015_04 |
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| ORD ID | ord-6e160dad9d544c888671cea1d32f8f85 |
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| Quellennotiz | uspto-grants-2015_04 |
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