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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 76083Erstellt: 25. Oktober 2026

Sodium Carbonate → (4-{4-[5-(6-Trifluoromethyl-pyridin-3-ylamino)-pyrazin-2-yl]-phenyl}-cyclohexyl)-acetic acid methyl ester

https://huagongshe.com/reaction/76083

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktSodium CarbonateHCID 10340—
EduktMethyl 2-[4-[4-(5-bromopyridin-2-yl)phenyl]cyclohexyl]acetateHCID 66615782—
Edukt(5-Bromopyrazin-2-yl)-(6-trifluoromethyl-pyridin-3-yl)-amineHCID 86634697—
KatalysatorHCID 178418397HCID 178418397—
Lösungsmittel1,2-DimethoxyethaneHCID 8071—
Produkt(4-{4-[5-(6-Trifluoromethyl-pyridin-3-ylamino)-pyrazin-2-yl]-phenyl}-cyclohexyl)-acetic acid methyl esterHCID 66615921—

Reaktionsbedingungen

Temperatur130 °C

Reaktionsschritte

A solution of (5-Bromopyrazin-2-yl)-(6-trifluoromethyl-pyridin-3-yl)-amine (0.072 g) and {4-[4-(5-bromo-pyridin-2-yl)-phenyl]-cyclohexyl}-acetic acid methyl ester (0.087 g) in 2 Ml DME was charged with 2 M sodium carbonate (1 Ml) and Pd(PPh3)4 (0.027 g, 0.1 equiv). The biphasic mixture was sparged with nitrogen for 3 min, then stirred at 130° C. under microwave heating for 30 min. The reaction was partitioned between EtOAc and water, and the organic extracts were dried over magnesium sulphate and concentrated in vacuo. Purification by silica gel chromatography (33% EtOAc in hexanes) afforded the title compound: (M+H)+471.2.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08835451B2
Quelldatensatzuspto-grants-2014_09
ORD IDord-9737d4bd15de43ed8bf00e5194056ba7
Quellennotizuspto-grants-2014_09