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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2276123Generated: October 26, 2026

2-Aminothiazole → 2-(2,4-Dichlorophenoxy)-5-fluoro-1-nitrobenzene

https://huagongshe.com/reaction/2276123

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-AminothiazoleHCID 2155—
Reactant2,4-DichlorophenolHCID 8449—
Reactant2,5-DifluoronitrobenzeneHCID 67767—
Reactant2-(2,4-Dichlorophenoxy)-5-fluoroanilineHCID 29780019—
ProductN-[2-(2,4-Dichlorophenoxy)-5-fluorophenyl]-N'-(thiazol-2-yl)ureaHCID 5973314176%
Product2-(2,4-Dichlorophenoxy)-5-fluoro-1-nitrobenzeneHCID 6699883078%

Reaction Steps

2-(2,4-Dichlorophenoxy)-5-fluoro-1-nitrobenzene (1.17 g, 78%) was prepared from 2,4-dichlorophenol (0.89 g, 5.5 mmol) and 2,5-difluoro-1-nitrobenzene (0.8 g, 5.0 mmol) following the general procedure A. This compound was reduced to 2-(2,4-dichlorophenoxy)-5-fluoroaniline (0.68 g, 64%) following the general procedure B. N-[2-(2,4-Dichlorophenoxy)-5-fluorophenyl]-N′-(thiazol-2-yl)urea (150 mg, 76%) was prepared from 2-(2,4-dichlorophenoxy)-5-fluoroaniline (135 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-1280d7815a3e4277b7a486c932bc3049
Source noteuspto-grants-2015_09