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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 598939Erstellt: 25. Oktober 2026

2-Aminothiazole → 2-(2-Methylsulfanylphenoxy)-1-nitrobenzene

https://huagongshe.com/reaction/598939

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Edukt2-AminothiazoleHCID 2155—
Edukto-(Methylthio)phenolHCID 61261—
Edukt1-Fluoro-2-nitrobenzeneHCID 73895—
Edukt2-(2-Methylsulfanylphenoxy)anilineHCID 59783707—
ProduktN-[2-(2-Methylsulfanylphenoxy)phenyl]-N'-(thiazol-2-yl)ureaHCID 5973270165%
Produkt2-(2-Methylsulfanylphenoxy)-1-nitrobenzeneHCID 5978361568%

Reaktionsschritte

2-(2-Methylsulfanylphenoxy)-1-nitrobenzene (0.88 g, 68%) was prepared from 2-hydroxythioanisole (0.77 g, 5.5 mmol) and 1-fluoro-2-nitrobenzene (0.71 g, 5.0 mmol) following the general procedure A. This was reduced to 2-(2-methylsulfanylphenoxy)aniline (0.53 g, 68%) following general procedure B. N-[2-(2-Methylsulfanylphenoxy)phenyl]-N′-(thiazol-2-yl)urea (115 mg, 65%) was prepared from 2-(2-methylsulfanylphenoxy)aniline (115 mg, 0.5 mmol) and 2-aminothiazole (60 mg, 0.6 mmol) following the general procedure D.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07897628B2
Quelldatensatzuspto-grants-2011_03
ORD IDord-1e8082bf430745fdb52a991d0e08f7ff
Quellennotizuspto-grants-2011_03