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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 571511Erstellt: 26. Oktober 2026

Diisopropylethylamine → methyl 4-{3-(cyanomethyl)-3-[4-(1H-pyrrolo[2,3-b]pyridin-4-yl)-1H-pyrazol-1-yl]azetidin-1-yl}-3-fluorobenzoate

https://huagongshe.com/reaction/571511

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktDiisopropylethylamineHCID 81531—
EduktSodium BicarbonateHCID 516892—
EduktMethyl 3,4-difluorobenzoateHCID 2775358—
EduktHCID 86675750HCID 86675750—
LösungsmittelN-methyl-2-pyrrolidoneHCID 13387—
Produktmethyl 4-{3-(cyanomethyl)-3-[4-(1H-pyrrolo[2,3-b]pyridin-4-yl)-1H-pyrazol-1-yl]azetidin-1-yl}-3-fluorobenzoateHCID 7114370633%

Reaktionsbedingungen

Temperatur130 °C

Reaktionsschritte

N,N-Diisopropylethylamine (1.6 mL, 9.5 mmol) was added to {3-[4-(1H-pyrrolo[2,3-b]pyridin-4-yl)-1H-pyrazol-1-yl]azetidin-3-yl}acetonitrile TFA salt (2.4 mmol) and methyl 3,4-difluorobenzoate (0.41 g, 2.4 mmol) (Aldrich, Cat. #: 594717) in N-methylpyrrolidinone (NMP) (5.0 mL). The reaction mixture was stirred at 130° C. overnight. The reaction mixture was worked up with saturated aqueous NaHCO3, extracted with ethyl acetate (3×20 mL). The combined organic layers were washed with brine, dried over MgSO4, filtered and concentrated under reduced pressure. The residue was purified by flash chromatography on a silica gel column with methanol in dichloromethane (0-5%) to afford the desired product (0.34 g, 33%). LCMS (M+H)+: m/z=431.1.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS09023840B2
Quelldatensatzuspto-grants-2015_05
ORD IDord-78532a02207d41af9cd1f76d05dafc4e
Quellennotizuspto-grants-2015_05