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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1983286Generated: October 26, 2026

2-Aminothiazole → 2-(3,5-Dimethylphenylsulfanyl)nitrobenzene

https://huagongshe.com/reaction/1983286

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-AminothiazoleHCID 2155—
Reactant1-Fluoro-2-nitrobenzeneHCID 73895—
Reactant3,5-DimethylbenzenethiolHCID 117548—
Reactant2-((3,5-Dimethylphenyl)thio)anilineHCID 66998967—
Product1-(Thiazol-2-yl)ureaHCID 1678170874%
Product2-(3,5-Dimethylphenylsulfanyl)nitrobenzeneHCID 6699901778%

Reaction Steps

2-(3,5-Dimethylphenylsulfanyl)nitrobenzene (1.01 g, 78%) was prepared from 3,5-dimethylthiophenol (0.76 g, 5.5 mmol) and 2-fluoronitrobenzene (0.71 g, 5.0 mmol) following the general procedure A. This compound was reduced to 2-(3,5-dimethylphenylsulfanyl)-aniline (0.64 g, 72%) following the general procedure B. N-[2-3,5-Dimethylphenylsulfanyl)-phenyl]-N′-(thiazol-2-yl)urea (131 mg; 74%) was prepared from 2-(3,5-dimethylphenyl-sulfanyl)aniline (115 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-6ab0f95507a24a36a404e275372fe87e
Source noteuspto-grants-2009_06