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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 131844Generated: October 25, 2026

2-Aminothiazole → Benzene, 1-fluoro-2-[(2-nitrophenyl)thio]-

https://huagongshe.com/reaction/131844

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-AminothiazoleHCID 2155—
Reactant1-Fluoro-2-nitrobenzeneHCID 73895—
Reactant2-FluorothiophenolHCID 520216—
Reactant2-(2-Fluorophenylsulfanyl)anilineHCID 11850357—
ProductBenzene, 1-fluoro-2-[(2-nitrophenyl)thio]-HCID 1185028783%
ProductHCID 59733001HCID 5973300175%

Reaction Steps

2-(2-Fluorophenylsulfanyl)nitrobenzene (1.03 g, 83%) was prepared from 2-fluorothiophenol (0.70 g, 5.5 mmol) and 2-fluoronitrobenzene (0.71 g, 5.0 mmol) following the general procedure A. This compound was reduced to 2-(2-fluorophenylsulfanyl)aniline (0.65 g, 72%) following general procedure B. N-[2-(2-Fluorophenylsulfanyl)phenyl]-N′-(thiazol-2-yl)urea (129 mg, 75%) was prepared from 2-(2-fluorophenylsulfanyl)aniline (107 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 numberUS07384967B2
Source datasetuspto-grants-2008_06
ORD IDord-782ed4d5a4c34964901422f06cd6ca0d
Source noteuspto-grants-2008_06