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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 131853Erstellt: 25. Oktober 2026

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

https://huagongshe.com/reaction/131853

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Edukt2-AminothiazoleHCID 2155—
Edukt1-Fluoro-2-nitrobenzeneHCID 73895—
EduktCyclopentanemethanolHCID 77195—
Edukt2-(Cyclopentylmethoxy)anilineHCID 19754712—
ProduktN-[2-(Cyclopentylmethoxy)phenyl]-N'-(thiazol-2-yl)ureaHCID 5973272060%
Produkt2-(Cyclopentylmethoxy)-1-nitrobenzeneHCID 6699890480%

Reaktionsschritte

2-(Cyclopentylmethoxy)-1-nitrobenzene (443 mg, 80%) was prepared from cyclopentanemethanol (0.32 ml, 3.0 mmol) and 1-fluoro-2-nitrobenzene (0.36 g, 2.5 mmol) following the general procedure G. This was reduced to 2-(cyclopentylmethoxy)aniline (268 mg, 70%) following general procedure B. N-[2-(Cyclopentylmethoxy)phenyl]-N′-(thiazol-2-yl)urea (286 mg, 60%) was prepared from 2-(cyclopentylmethoxy)aniline (0.25 g, 1.5 mmol) and 2-aminothiazole (150 mg, 1.5 mmol) following the general procedure D.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07384967B2
Quelldatensatzuspto-grants-2008_06
ORD IDord-92b0c447208c44e08a1489467c195453
Quellennotizuspto-grants-2008_06