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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 559840Generated: October 26, 2026

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

https://huagongshe.com/reaction/559840

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-AminothiazoleHCID 2155—
Reactant4-IsopropylphenolHCID 7465—
Reactant1-Fluoro-2-nitrobenzeneHCID 73895—
Reactant2-(4-Isopropylphenoxy)anilineHCID 26189126—
ProductN-[2-(4-Isopropylphenoxy)phenyl]-N'-(thiazol-2-yl)ureaHCID 5973279170%
Product2-(4-Isopropylphenoxy)-1-nitrobenzeneHCID 6699897075%

Reaction Steps

2-(4-Isopropylphenoxy)-1-nitrobenzene (0.95 g, 75%) was prepared from 4-isopropylphenol (0.68 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-isopropylphenoxy)aniline (0.34 g, 60%, 2.5 mmol scale) following general procedure B. N-[2-(4-Isopropylphenoxy)phenyl]-N′-(thiazol-2-yl)urea (247 mg, 70%) was prepared from 2-(4-isopropylphenoxy)aniline (227 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 numberUS08063081B2
Source datasetuspto-grants-2011_11
ORD IDord-2a9e41004e5d42cab1bcc58c7eb1ddb2
Source noteuspto-grants-2011_11