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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 910693Erstellt: 23. Oktober 2026

2-(Tri-n-butylstannyl)thiophene → 1-Methyl-4-(5-thiophen-2-yl-pyridin-3-yl)-piperazine

https://huagongshe.com/de/reaction/910693

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Edukt2-(Tri-n-butylstannyl)thiopheneHCID 2779373—
Edukt1-(5-Bromopyridin-3-yl)-4-methylpiperazineHCID 53485314—
KatalysatorHCID 178418397HCID 178418397—
Lösungsmittel1,4-DioxaneHCID 31275—
Produkt1-Methyl-4-(5-thiophen-2-yl-pyridin-3-yl)-piperazineHCID 22632288—

Reaktionsbedingungen

Temperatur100 °C

Reaktionsschritte

To a vial was added 1-(5-bromo-pyridin-3-yl)-4-methyl-piperazine (47 mg, 0.13 mmol), Pd(PPh3)4 (34 mg), 2-thienyltributylstannane (67 mg, 0.15 mmol) and dioxane (1 mL). The resulting mixture was heated at 100° C. for 24 hrs. The resulting mixture was extracted with EtOAc. The organic layer was dried and concentrated, and the residue was purified by preparative TLC (hexanes/EtOAc) to yield the title compound as a solid.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08022209B2
Quelldatensatzuspto-grants-2011_09
ORD IDord-f590971f92df40c184810059889b07ef
Quellennotizuspto-grants-2011_09