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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 23366Erstellt: 23. Oktober 2026

2-Furancarboxylic acid → HCID 178523861, Verbindung

https://huagongshe.com/de/reaction/23366

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Edukt2-Furancarboxylic acidHCID 6919—
Edukt1,1'-CarbonyldiimidazoleHCID 68263—
EduktHCID 178511781HCID 178511781—
ProduktHCID 178523861HCID 17852386194%

Reaktionsbedingungen

Temperatur22 °C

Reaktionsschritte

2-Furancarboxylic acid (12.6 mg, 0.11 mmol) was activated overnight at about 22° C. with carbonyldiimidazole (0.11 mmol, 0.2M in chloroform). 2-{(1S)-1-Amino-2-[indol-3-yl]ethyl}-4-phenyl-1H-imidazole (0.1 mmol, 0.5M in chloroform) was added to the media and the mixture was stirred for about 12 hours at about 22° C. Aminomethylated resin was then added (50-60 mg, 1.2 mmol/g, Novabiochem) in order to quench the excess of acylating agent for about 12 hours. Purification on silica gel pad (200 mg, Alltech) with ethyl acetate as eluent gave the expected product (37.2 mg, 94%). 1H-NMR (CDCl3, 100 MHz) δ: 8.36 (br s, 1H); 7.67-6.4 (m, 16H); 5.48 (qd, J=7.1 Hz, 1H); 3.6 (ABX system, 2H). LC/MS: m/z=397 (M+H).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS06852725B1
Quelldatensatzuspto-grants-2005_02
ORD IDord-53c35be4278545ed89106e250fee70d4
Quellennotizuspto-grants-2005_02