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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2276261Generated: October 29, 2026

2-Aminothiazole → HCID 59732983, compound

https://huagongshe.com/reaction/2276261

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-AminothiazoleHCID 2155—
Reactantm-Chloroperbenzoic acidHCID 70297—
ReactantHCID 66999062HCID 66999062—
ReactantHCID 66999204HCID 66999204—
ProductHCID 59732983HCID 5973298365%

Reaction Steps

3-Cyclopentanesulfanyl-4-nitrotoluene (0.47 g, 2.0 mmol) was oxidized to 3-cyclopentanesulfinyl-4-nitrotoluene (0.46 g, 91%) following general procedure R (using one equivalent of m-CPBA). 3-Cyclopentanesulfinyl-4-nitrotoluene was reduced to 2-cyclopentanesulfinyl-4-methyl-aniline (0.33 g, 81%) following general procedure C. 1-(2-Cyclopentanesulfinyl-4-methyl-phenyl)-3-thiazol-2-yl-urea (225 mg, 65%) was prepared from 2-cyclopentanesulfinyl-4-methyl-aniline (223 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 numberUSRE045670E1
Source datasetuspto-grants-2015_09
ORD IDord-4a7b5343f0434de5a8372eb62d565ec6
Source noteuspto-grants-2015_09