Zurück
HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 131973Erstellt: 24. Oktober 2026

2-Aminothiazole → 4-(2-Fluoro-6-methoxy-phenoxy)-3-nitrobenzaldehyde

https://huagongshe.com/de/reaction/131973

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Edukt2-AminothiazoleHCID 2155—
Edukt4-Fluoro-3-nitrobenzaldehydeHCID 598129—
Edukt2-Fluoro-6-methoxyphenolHCID 2737367—
Edukt5-Formyl-2-(2-fluoro-6-methoxy-phenoxy)-anilineHCID 86593084—
Produkt1-[2-(2-Fluoro-6-methoxy-phenoxy)-5-formyl-phenyl]-3-thiazol-2-yl-ureaHCID 5973295469%
Produkt4-(2-Fluoro-6-methoxy-phenoxy)-3-nitrobenzaldehydeHCID 8659308370%

Reaktionsschritte

4-(2-Fluoro-6-methoxy-phenoxy)-3-nitrobenzaldehyde (1.0 g, 70%) was prepared from 2-fluoro-6-methoxyphenol (0.78 g, 5.5 mmol) and 4-fluoro-3-nitrobenzaldehyde (0.84 g, 5.0 mmol) following the general procedure A. This was reduced to 5-formyl-2-(2-fluoro-6-methoxy-phenoxy)-aniline (0.57 g, 62%) following general procedure B. 1-[2-(2-Fluoro-6-methoxy-phenoxy)-5-formyl-phenyl]-3-thiazol-2-yl-urea (265 mg, 69%) was prepared from 5-formyl-2-(2-fluoro-6-methoxy-phenoxy)-aniline (261 mg, 1.0 mmol) and 2-aminothiazole (100 mg, 1.0 mmol) following the general procedure D.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07384967B2
Quelldatensatzuspto-grants-2008_06
ORD IDord-971efa14457b47c499e8f06cd1911d93
Quellennotizuspto-grants-2008_06