Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2276150Generated: October 27, 2026

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

https://huagongshe.com/reaction/2276150

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-AminothiazoleHCID 2155—
Reactant1-Fluoro-2-nitrobenzeneHCID 73895—
ReactantCyclopentanemethanolHCID 77195—
Reactant2-(Cyclopentylmethoxy)anilineHCID 19754712—
ProductN-[2-(Cyclopentylmethoxy)phenyl]-N'-(thiazol-2-yl)ureaHCID 5973272060%
Product2-(Cyclopentylmethoxy)-1-nitrobenzeneHCID 6699890480%

Reaction Steps

2-(Cyclopentylmethoxy)-1-nitrobenzene (443 mg, 80%) was prepared from cyclopentanemethanol (0.32 ml, 3.0 mmol) and 1-fluoro-2-nitrobenzene (0.36 g, 2.5 mmol) following the general procedure G. This was reduced to 2-(cyclopentylmethoxy)aniline (268 mg, 70%) following general procedure B. N-[2-(Cyclopentylmethoxy)phenyl]-N′-(thiazol-2-yl)-urea (286 mg, 60%) was prepared from 2-(cyclopentylmethoxy)aniline (0.25 g, 1.5 mmol) and 2-aminothiazole (150 mg, 1.5 mmol) following the general procedure D.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUSRE045670E1
Source datasetuspto-grants-2015_09
ORD IDord-3f1c94ab1e96470590b83212c076456e
Source noteuspto-grants-2015_09