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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1983231Generated: October 29, 2026

2-Aminothiazole → 1-(4-Methoxyphenoxy)-2-nitrobenzene

https://huagongshe.com/reaction/1983231

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-AminothiazoleHCID 2155—
Reactant4-MethoxyphenolHCID 9015—
Reactant1-Fluoro-2-nitrobenzeneHCID 73895—
Reactant2-(4-methoxyphenoxy)anilineHCID 361286—
Product1-(4-Methoxyphenoxy)-2-nitrobenzeneHCID 66815080%
ProductHCID 59733128HCID 5973312875%

Reaction Steps

2-(4-Methoxyphenoxy)-1-nitrobenzene (0.98 g, 80%) was prepared from 4-methoxyphenol (0.62 g, 5.0 mmol) and 1-fluoro-2-nitrobenzene (0.71 g, 5.0 mmol) following the general procedure A. This was reduced to 2-(4-methoxyphenoxy)aniline (0.32 g, 60%, 2.5 mmol scale) following the general procedure B. N-[2-(4-Methoxyphenoxy)phenyl)-N′-(thiazol-2-yl)urea (256 mg, 75%) was prepared from 2-(4-methoxyphenoxy)aniline (215 mg, 1.0 mmol) and 2-aminothiazole (100 mg, 1.0 mmol) following the general procedure D.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07541373B2
Source datasetuspto-grants-2009_06
ORD IDord-1ebd548f7dba40a5b5422cc4f0841870
Source noteuspto-grants-2009_06