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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 715006Erstellt: 24. Oktober 2026

Benzylethanolamine → 2-(2,6-Difluorophenyl)-5-(4-(2-(2-hydroxyethylamino)ethoxy)phenyl)oxazole-4-carboxamide

https://huagongshe.com/de/reaction/715006

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktBenzylethanolamineHCID 4348—
Edukt5-(4-(2-Chloroethoxy)phenyl)-2-(2,6-difluorophenyl)oxazole-4-carboxamideHCID 59587375—
Edukt2,4-bis(4-methoxyphenyl)-1H-imidazole-5-carboxamideHCID 59587424—
KatalysatorPalladiumHCID 23938—
LösungsmittelMethanolHCID 887—
Produkt2-(2,6-Difluorophenyl)-5-(4-(2-(2-hydroxyethylamino)ethoxy)phenyl)oxazole-4-carboxamideHCID 59587449—

Reaktionsschritte

The title compound was prepared by reaction of 5-(4-(2-chloroethoxy)phenyl)-2-(2,6-difluorophenyl)oxazole-4-carboxamide with 2-(benzylamino)ethanol, according to the procedure described in example S-1, step c, followed by deprotection with the H-cube hydrogenation system (full H2 mode, 10% Pd\C catalyst, 1 ml/min, 60° C., 0.05M in MeOH). 1H NMR (DMSO) δ 2.79 (2H, t), 3.17 (2H, t), 3.55 (2H, t), 4.20 (2H, t), 7.05-7.15 (2H, m), 7.35-7.45 (2H, m), 7.60-7.80 (3H, m), 8.20-8.30 (2H, m). LCMS (2) 2.17 min; m/z (ES+) 404.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS09187465B2
Quelldatensatzuspto-grants-2015_11
ORD IDord-d143a47dc0ed42388c8f27a320c2f2a9
Quellennotizuspto-grants-2015_11