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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 131782Erstellt: 25. Oktober 2026

2-Aminothiazole → 2-(2,3,4-Trimethoxybenzyloxy)-1-nitrobenzene

https://huagongshe.com/reaction/131782

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Edukt2-AminothiazoleHCID 2155—
Edukt1-Fluoro-2-nitrobenzeneHCID 73895—
Edukt(2,3,4-Trimethoxyphenyl)methanolHCID 123571—
Edukt2-(2,3,4-Trimethoxybenzyloxy)anilineHCID 66998842—
ProduktN-[2-(2,3,4-trimethoxybenzyloxy)phenyl]-N'-(thiazol-2-yl)ureaHCID 5973270765%
Produkt2-(2,3,4-Trimethoxybenzyloxy)-1-nitrobenzeneHCID 6699891072%

Reaktionsschritte

2-(2,3,4-Trimethoxybenzyloxy)-1-nitrobenzene (0.46 g, 72%) was prepared from 2,3,4-trimethoxybenzyl alcohol (0.35 ml, 2.0 mmol) and 1-fluoro-2-nitrobenzene (0.21 ml, 2.0 mmol) following the general procedure G. This was reduced to 2-(2,3,4-trimethoxybenzyloxy)aniline (0.26 g, 65%) following the general procedure B. N-[2-(2,3,4-trimethoxybenzyloxy)phenyl]-N′-(thiazol-2-yl)urea (240 mg, 65%) was prepared from 2-(2,3,4-trimethoxybenzyloxy)aniline (0.26 g, 0.9 mmol) and 2-aminothiazole (140 mg, 1.4 mmol) following the general procedure D.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07384967B2
Quelldatensatzuspto-grants-2008_06
ORD IDord-c1fe1c11381f4ac6b6a7915d380ed534
Quellennotizuspto-grants-2008_06