Zurück
HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 45153Erstellt: 23. Oktober 2026

2,2'-Bipyridine → 1,5-Dicyclopropyl-3-(2,5-dimethyl-pyrrol-1-yl)-1H-pyrazole

https://huagongshe.com/de/reaction/45153

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Edukt2,2'-BipyridineHCID 1474—
EduktSodium CarbonateHCID 10340—
Edukt5-Cyclopropyl-3-(2,5-dimethyl-pyrrol-1-yl)-1H-pyrazoleHCID 59394660—
KatalysatorCupric acetateHCID 8895—
Lösungsmittel1,2-DichloroethaneHCID 11—
Produkt1,5-Dicyclopropyl-3-(2,5-dimethyl-pyrrol-1-yl)-1H-pyrazoleHCID 59394790104,2%

Reaktionsbedingungen

Temperatur70 °C

Reaktionsschritte

A suspension of copper (II) acetate (0.902 g, 4.97 mmol) and 2,2′-bipyridine (0.776 g, 4.97 mmol) in DCE (20 mL) is stirred at 70° C. for 15 min, then transferred to a suspension of cyclopropyl trifluoroborate potassium salt (1.47 g, 9.94 mmol) and 5-Cyclopropyl-3-(2,5-dimethyl-pyrrol-1-yl)-1H-pyrazole (1 g, 4.97 mmol), and sodium carbonate (1.053 g, 9.94 mmol) in DCE (40 mL). The resulting dark-green mixture is stirred at 70° C. for 24 h. T The reaction mixture is partitioned between EtOAc and 1N HCl. The aqueous layer is extracted with EtOAc. The combined organic layers are washed with brine, dried (Na2SO4) and concentrated. The residue (1.64 g) is purified by ISCO (EtOAc-heptane 0-30%) to provide the desired product (1.25 g) as a colorless oil. MS (ESI) m/z 242.3 (M+1).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08541432B2
Quelldatensatzuspto-grants-2013_09
ORD IDord-d2d5fd8e56d141a08b39d578e86e99af
Quellennotizuspto-grants-2013_09