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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 131849Generated: October 29, 2026

2-Aminothiazole → HCID 10263334, compound

https://huagongshe.com/reaction/131849

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-AminothiazoleHCID 2155—
Reactant1-Fluoro-2-nitrobenzeneHCID 73895—
ReactantHCID 15211606HCID 15211606—
ReactantHCID 178418616HCID 178418616—
ProductHCID 10263334HCID 1026333460%
ProductHCID 59732887HCID 5973288760%

Reaction Steps

2-(2-Pyridylsulfanyl)nitrobenzene (0.70 g, 60%) was prepared from 2-mercaptopyridine (0.61 g, 5.5 mmol) and 2-fluoronitrobenzene (0.71 g, 5.0 mmol) following the general procedure A. This compound was reduced to 2-(2-pyridylsulfanyl)aniline (0.37 g, 62%) following general procedure B. N-[2-(2-Pyridylsulfanyl)phenyl]-N′-(thiazol-2-yl)urea (98 mg, 60%) was prepared from 2-(2-pyridylsulfanyl)aniline (101 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 numberUS07384967B2
Source datasetuspto-grants-2008_06
ORD IDord-10fec773f3364e4e92512c7602f529ff
Source noteuspto-grants-2008_06