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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 598923Generated: October 31, 2026

2-Aminothiazole → 4-(2-nitrophenoxy)benzonitrile

https://huagongshe.com/reaction/598923

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-AminothiazoleHCID 2155—
Reactant4-CyanophenolHCID 13019—
Reactant1-Fluoro-2-nitrobenzeneHCID 73895—
Reactant4-(2-aminophenoxy)benzonitrileHCID 815649—
Product4-(2-nitrophenoxy)benzonitrileHCID 921343569%
ProductHCID 59732941HCID 5973294165%

Reaction Steps

2-(4-Cyanophenoxy)-1-nitrobenzene (0.82 g, 69%) was prepared from 4-cyanophenol (0.66 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-(4-cyanophenoxy)aniline (0.47 g, 65%) following general procedure B. N-[2-(4-Cyanophenoxy)phenyl]-N′-thiazolylurea (110 mg, 65%) was prepared from 2-(4-cyanophenoxy)aniline (105 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 numberUS07897628B2
Source datasetuspto-grants-2011_03
ORD IDord-983699721d204a3095d1f01d289375b9
Source noteuspto-grants-2011_03