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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 131839Generated: October 29, 2026

2-Aminothiazole → HCID 66998272, compound

https://huagongshe.com/reaction/131839

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-AminothiazoleHCID 2155—
Reactant2,3-DimethoxyphenolHCID 78828—
Reactant1,2,4-Trifluoro-3-nitrobenzeneHCID 3016321—
ReactantHCID 66998752HCID 66998752—
ReactantHCID 66999025HCID 66999025—
ProductHCID 59732691HCID 5973269189%
ProductHCID 66998272HCID 6699827290.3%

Reaction Steps

4,5-Difluoro-2-(2,3-dimethoxyphenoxy)-1-nitrobenzene (1.4 g, 90.3%) was prepared from 2,3-dimethoxyphenol (0.85 g, 5.5 mmol) and 1,3,4-trifluoronitrobenzene (0.885 g, 5.0 mmol) following the general procedure F. The product was then reduced to 2-(2-methoxyphenoxy)-4,5-difluoroaniline (1.35 g, 96.1%) following general procedure B. N-[4,5-Difluoro-2-(2,3-dimethoxyphenoxy)phenyl]-N′-(thiazol-2-yl)urea (0.181 g, 89%) was prepared from 2-(2,3-dimethoxyphenoxy)-4,5-difluoroaniline (0.140 g, 0.5 mmol) and 2-aminothiazole (0.060 g, 0.6 mmol) following the general procedure D.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07384967B2
Source datasetuspto-grants-2008_06
ORD IDord-3986927026ee44d4bf76fa60885094cf
Source noteuspto-grants-2008_06