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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 598982Generated: October 25, 2026

2-Aminothiazole → 1-(Cyclopentyloxy)-2-nitrobenzene

https://huagongshe.com/reaction/598982

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-AminothiazoleHCID 2155—
ReactantCyclopentanolHCID 7298—
Reactant1-Fluoro-2-nitrobenzeneHCID 73895—
Reactant2-(Cyclopentyloxy)anilineHCID 6485398—
Product1-(Cyclopentyloxy)-2-nitrobenzeneHCID 2216447380%
ProductN-(2-Cyclopentyloxyphenyl)-N'-(thiazol-2-yl)ureaHCID 5973294070%

Reaction Steps

2-(Cyclopentyloxy)-1-nitrobenzene (1.04 g, 80%) was prepared from cyclopentanol (0.46 ml, 5.0 mmol) and 1-fluoro-2-nitrobenzene (0.71 g, 5.0 mmol) following the general procedure G. This was reduced to 2-(cyclopentyloxy)aniline (0.30 g, 68%, 2.5 mmol scale) following general procedure B. N-(2-Cyclopentyloxyphenyl)-N′-(thiazol-2-yl)urea (212 mg, 70%) was prepared from 2-(cyclopentyloxy)aniline (177 mg, 1.0 mmol) and 2-aminothiazole (100 mg, 1.0 mmol) following the general procedure D.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07897628B2
Source datasetuspto-grants-2011_03
ORD IDord-c095b2be352943a3b87b1791fcaba1a0
Source noteuspto-grants-2011_03