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HRID 1713003Erstellt: 26. Oktober 2026

Potassium tert-butoxide → 2-Chloro-5H-pyrrolo[2,3-B]pyrazine

https://huagongshe.com/reaction/1713003

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktPotassium tert-butoxideHCID 23665647—
Edukt5-Chloro-3-(triethyl-silanylethynyl)-pyrazin-2-ylamineHCID 59463522—
LösungsmittelN-methyl-2-pyrrolidoneHCID 13387—
LösungsmittelSodium chloride; waterHCID 57417360—
Produkt2-Chloro-5H-pyrrolo[2,3-B]pyrazineHCID 45789638—

Reaktionsbedingungen

Temperatur80 °C

Reaktionsschritte

A solution of potassium tert-butoxide (1 g, 4.5 mM) in N-methylpyrrolidone (3 ml) was heated to 80° C. under nitrogen. A solution of 5-chloro-3-(triethyl-silanylethynyl)-pyrazin-2-ylamine (3) (1.2 g, 4.5 mmol) in N-methylpyrrolidone (10 ml) was added dropwise. The reaction mixture was stirred at 80° C. for a further fifty minutes and then the reaction mixture was allowed to cool to room temperature. Brine (10 ml) was added to the reaction mixture and extracted with ethyl acetate (5×20 ml). The combined organics were washed with brine, dried over magnesium sulfate and concentrated in vacuo to afford the title compound as a solution in N-methylpyrrolidone. MS(ES+): 154

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07795259B2
Quelldatensatzuspto-grants-2010_09
ORD IDord-ca22afe92f4843c3b7c86fc0434c43e7
Quellennotizuspto-grants-2010_09