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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1983246Generated: October 29, 2026

2-Aminothiazole → HCID 245943, compound

https://huagongshe.com/reaction/1983246

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-AminothiazoleHCID 2155—
Reactant3-(Trifluoromethyl)phenolHCID 7376—
Reactant1-Fluoro-2-nitrobenzeneHCID 73895—
Reactant2-[3-(Trifluoromethyl)phenoxy]benzenamineHCID 19626916—
ProductHCID 245943HCID 24594365%
ProductHCID 59733082HCID 5973308262%

Reaction Steps

2-[3-(Trifluoromethyl)phenoxy]-1-nitrobenzene (0.92 g, 65%) was prepared from 3-hydroxybenzotrifluoride (0.89 g, 5.5 mmol) and 1-fluoro-2-nitrobenzene (0.71 g, 5.0 mmol) following the general procedure A. This was reduced to 2-[3-(trifluoromethyl)phenoxy]aniline (0.56 g, 68%) following general procedure B. N-[2-(3-Trifluoromethylphenoxy)phenyl]-N′-(thiazol-2-yl)urea (120 mg, 62%) was prepared from 2-[3-(trifluoromethyl)phenoxy]aniline (127 mg, 0.5 mmol) and 2-aminothiazole (60 mg, 0.6 mmol) following the general procedure D.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07541373B2
Source datasetuspto-grants-2009_06
ORD IDord-1d217c2085014840b78a89629c67b5d0
Source noteuspto-grants-2009_06