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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 560002Generated: October 29, 2026

2-Aminothiazole → HCID 59732679, compound

https://huagongshe.com/reaction/560002

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-AminothiazoleHCID 2155—
ReactantCyclopentanolHCID 7298—
ReactantBenzene, 2-fluoro-4-methyl-1-nitro-HCID 67966—
Reactant2-(Cyclopentyloxy)-4-methylanilineHCID 24709816—
ProductHCID 59732679HCID 5973267970%
ProductHCID 66998953HCID 6699895362%

Reaction Steps

3-Cyclopentyloxy-4-nitrotoluene (0.68 g, 62%) was prepared from cyclopentanol and 3-fluoro-4-nitrotoluene (0.77 g, 5.0 mmol) following the general procedure G. This was reduced to 2-cyclopentyloxy-4-methyl-aniline (0.43 g, 70%) following general procedure C. 1-(2-Cyclopentyloxy-4-methyl-phenyl)-3-thiazol-2-yl-urea (220 mg, 70%) was prepared from 2-cyclopentyloxy-4-methyl-aniline (191 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 numberUS08063081B2
Source datasetuspto-grants-2011_11
ORD IDord-75a2d834f09a41da9a476aa6bca91dba
Source noteuspto-grants-2011_11