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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2276142Generated: October 30, 2026

2-Aminothiazole → 2-(2-Chloro-4-fluorophenylsulfanyl)nitrobenzene

https://huagongshe.com/reaction/2276142

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-AminothiazoleHCID 2155—
Reactant1-Fluoro-2-nitrobenzeneHCID 73895—
Reactant2-Chloro-4-fluorothiophenolHCID 519446—
Reactant2-(2-Chloro-4-fluorophenylsulfanyl)anilineHCID 66998238—
ProductN-[2-(2-Chloro-4-fluorophenylsulfanyl)phenyl]-N'-(thiazol-2-yl)ureaHCID 5973275276%
Product2-(2-Chloro-4-fluorophenylsulfanyl)nitrobenzeneHCID 6699896080%

Reaction Steps

2-(2-Chloro-4-fluorophenylsulfanyl)nitrobenzene (1.13 g, 80%) was prepared from 2-chloro-4-fluorothiophenol (0.89 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-chloro-4-fluorophenylsulfanyl)aniline (0.76 g, 75%) following the general procedure B. N-[2-(2-Chloro-4-fluorophenylsulfanyl)phenyl]-N′-(thiazol-2-yl)urea (144 mg, 76%) was prepared from 2-(2-chloro-4-fluorophenylsulfanyl)aniline (126 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 numberUSRE045670E1
Source datasetuspto-grants-2015_09
ORD IDord-2a309c0067e64442b869064d1fa54f70
Source noteuspto-grants-2015_09