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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 595797Erstellt: 25. Oktober 2026

1,2-Dichloroethane → 4-(2,2-Difluoro-1-phenylethylcarbamoyl)-3-fluorophenylboronic acid

https://huagongshe.com/reaction/595797

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Edukt1,2-DichloroethaneHCID 11—
EduktCitric AcidHCID 311—
EduktDiisopropylethylamineHCID 81531—
EduktHOAtHCID 181649—
Edukt4-Carboxy-3-fluorophenylboronic acidHCID 2763201—
Edukt2,2-Difluoro-1-phenylethan-1-amineHCID 45282641—
LösungsmittelDimethylformamideHCID 6228—
LösungsmittelTetrahydrofuranHCID 8028—
Produkt4-(2,2-Difluoro-1-phenylethylcarbamoyl)-3-fluorophenylboronic acidHCID 123534983—

Reaktionsschritte

To a solution of 4-borono-2-fluorobenzoic acid (200 mg, 1.087 mmol), 2,2-difluoro-1-phenylethanamine (232 mg, 1.196 mmol), and DIEA (0.570 mL, 3.26 mmol) in THF (3.866 mL) and DMF (0.483 mL) was added HOAt (296 mg, 2.175 mmol) and EDC (521 mg, 2.72 mmol). After 3 h stirring at room temperature, 10% citric acid solution was added (pH ˜3) and extracted with 2-methyl THF and EtOAc (1:1). The organic layers were dried over anhydrous Na2SO4, filtered, and concentrated. The crude 4-(2,2-difluoro-1-phenylethylcarbamoyl)-3-fluorophenylboronic acid was obtained (90%) and used for the next step without purification. LCMS (m/z): 375.3 (MH+), 0.48 min.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS09242996B2
Quelldatensatzuspto-grants-2016_01
ORD IDord-10da6daac0da476486f9959ec4a2ca54
Quellennotizuspto-grants-2016_01