Zurück
HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 2276147Erstellt: 25. Oktober 2026

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

https://huagongshe.com/reaction/2276147

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Edukt2-AminothiazoleHCID 2155—
EduktCyclopentanolHCID 7298—
Edukt1-Fluoro-2-nitrobenzeneHCID 73895—
Edukt2-(Cyclopentyloxy)anilineHCID 6485398—
Produkt1-(Cyclopentyloxy)-2-nitrobenzeneHCID 2216447380%
ProduktN-(2-Cyclopentyloxyphenyl)-N'-(thiazol-2-yl)ureaHCID 5973294070%

Reaktionsschritte

2-(Cyclopentyloxy)-1-nitrobenzene (1.04 g, 80%) was prepared from cyclopentanol (0.46 ml, 5.0 mmol) and 1-fluoro-2-nitrobenzene (0.71 g, 5.0 mmol) following the general procedure G. This was reduced to 2-(cyclopentyloxy)aniline (0.30 g, 68%, 2.5 mmol scale) following general procedure B. N-(2-Cyclopentyloxyphenyl)-N′-(thiazol-2-yl)urea (212 mg, 70%) was prepared from 2-(cyclopentyloxy)aniline (177 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
PatentnummerUSRE045670E1
Quelldatensatzuspto-grants-2015_09
ORD IDord-a2fdc6f889d64b168fe8a51f0c5cec98
Quellennotizuspto-grants-2015_09