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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 2184030Erstellt: 25. Oktober 2026

3-bromo-7-(trifluoromethyl)imidazo[1,2-a]pyrimidine → 2'-Fluoro-5'-(7-trifluoromethylimidazo[1,2-alpha]pyrimidin-3-yl)biphenyl-4-carbonitrile

https://huagongshe.com/reaction/2184030

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Edukt3-bromo-7-(trifluoromethyl)imidazo[1,2-a]pyrimidineHCID 11391462—
Edukt5'-(5,5-Dimethyl[1,3,2]dioxaborinan-2-yl)-2'-fluorobiphenyl-4-carbonitrileHCID 22285322—
Produkt2'-Fluoro-5'-(7-trifluoromethylimidazo[1,2-alpha]pyrimidin-3-yl)biphenyl-4-carbonitrileHCID 10271229—

Reaktionsschritte

3-Bromo-7-trifluoromethylimidazo[1,2-α]pyrimidine was coupled with 5′-(5,5-dimethyl-[1,3,2]dioxaborinan-2-yl)-2′-fluorobiphenyl-4-carbonitrile as described in Example 65 to give 2′-fluoro-5′-(7-trifluoromethylimidazo[1,2-α]pyrimidin-3-yl)biphenyl-4-carbonitrile as a yellow solid: δH (360 MHz, CDCl3) 7.26 (1H, d, J 7), 7.44 (1H, dd, J 8 and 8), 7.55-7.63 (2H, m), 7.70 (2H, dd, J 7 and 1), 7.79 (2H, dd, J 7 and 1), 8.11 (1H, s), 8.74 (1H, d, J 7); m/z (ES+) 383 (M++H).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS06900215B2
Quelldatensatzuspto-grants-2005_05
ORD IDord-39f6408f5d4844cc80c72f030318081d
Quellennotizuspto-grants-2005_05