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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1092080Erstellt: 26. Oktober 2026

Toluene → HCID 178489801, Verbindung

https://huagongshe.com/reaction/1092080

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktTolueneHCID 1140—
EduktMethyl 5-chloropyrazine-2-carboxylateHCID 406081—
EduktTrimethylaluminumHCID 16682925—
EduktHCID 178489815HCID 178489815—
ProduktHCID 178489801HCID 17848980163%

Reaktionsschritte

Trimethylaluminium (2M in toluene, 9.64 ml, 19.28 mmol) was added dropwise to a stirred suspension of 5-[2-(3,5-dimethoxyphenyl)ethyl]-2H-pyrazol-3-amine (1.91 g, 7.71 mmol) and methyl 5-chloropyrazine-2-carboxylate (1.33 g, 7.71 mmol) in anhydrous toluene (38.6 ml) at ambient temperature. The resulting solution was then stirred under nitrogen at ambient temperature for 18 h. The reaction was incomplete so the temperature was increased to 60° C. and the reaction mixture was stirred for a further 3 h. The reaction mixture was quenched with methanol (10 mL) and HCl (2M aqueous solution). The mixture was diluted with EtOAc (100 mL) and water (250 mL) and then acidified with HCl (2N aqueous solution). The organic layer was removed and the aqueous further extracted with EtOAc (2×100 mL). The combined organics were washed with water (200 mL), brine (200 mL) dried over MgSO4 and concentrated under reduced pressure. Upon concentration a precipitate formed. The precipitate was collected by filtration, washed with MeOH (10 mL) and air dried to afford the desired compound (1.88 g, 63%) as a yellow solid, which was used without further purification.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08129391B2
Quelldatensatzuspto-grants-2012_03
ORD IDord-a50b1412f71d407a99745ed00a378867
Quellennotizuspto-grants-2012_03