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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1515508Erstellt: 26. Oktober 2026

3-Aminobenzamide → 2-(3-Carbamoylphenylamino)-2-(3-ethoxy-4-fluorophenyl)acetic acid

https://huagongshe.com/reaction/1515508

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Edukt3-AminobenzamideHCID 1645—
EduktGlyoxylic acid, monohydrateHCID 15620607—
Edukt3-Ethoxy-4-fluorobenzeneboronic acidHCID 44558174—
LösungsmittelDimethylformamideHCID 6228—
LösungsmittelAcetonitrileHCID 6342—
Produkt2-(3-Carbamoylphenylamino)-2-(3-ethoxy-4-fluorophenyl)acetic acidHCID 5947942860,2%

Reaktionsbedingungen

Temperatur55 °C

Reaktionsschritte

A mixture of 3-aminobenzamide (68 mg, 0.5 mmol), 9B (92 mg, 0.5 mmol) and glyoxylic acid monohydrate (46 mg, 0.5 mmol) in acetonitrile (3.0 mL) and DMF (0.8 mL) was heated at 55° C. for 18 h. After removal of solvent, the crude was purified by silica gel column chromatography eluting with gradient methanol in methylene chloride to give 9C as a solid (100 mg, 60% yield). 1H NMR (400 MHz, Methanol-d4) δ ppm 1.25 (t, J=6.81 Hz, 3H) 3.96 (m, 2H) 5.03 (s, 1H) 6.70 (d, J=7.91 Hz, 1H) 6.96-7.08 (m, 5H) 7.15 (dd, J=8.35, 1.76 Hz, 1H); LC-MS 333 (M+H).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08222453B2
Quelldatensatzuspto-grants-2012_07
ORD IDord-c5cb696f8089423b91dbb7e9273cd470
Quellennotizuspto-grants-2012_07