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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 599106Generated: October 26, 2026

2-Aminothiazole → 4-(2-Fluoro-6-methoxy-phenoxy)-3-nitrobenzaldehyde

https://huagongshe.com/reaction/599106

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-AminothiazoleHCID 2155—
Reactant4-Fluoro-3-nitrobenzaldehydeHCID 598129—
Reactant2-Fluoro-6-methoxyphenolHCID 2737367—
Reactant5-Formyl-2-(2-fluoro-6-methoxy-phenoxy)-anilineHCID 86593084—
Product1-[2-(2-Fluoro-6-methoxy-phenoxy)-5-formyl-phenyl]-3-thiazol-2-yl-ureaHCID 5973295469%
Product4-(2-Fluoro-6-methoxy-phenoxy)-3-nitrobenzaldehydeHCID 8659308370%

Reaction Steps

4-(2-Fluoro-6-methoxy-phenoxy)-3-nitrobenzaldehyde (1.0 g, 70%) was prepared from 2-fluoro-6-methoxyphenol (0.78 g, 5.5 mmol) and 4-fluoro-3-nitrobenzaldehyde (0.84 g, 5.0 mmol) following the general procedure A. This was reduced to 5-formyl-2-(2-fluoro-6-methoxy-phenoxy)-aniline (0.57 g, 62%) following general procedure B. 1-[2-(2-Fluoro-6-methoxy-phenoxy)-5-formyl-phenyl]-3-thiazol-2-yl-urea (265 mg, 69%) was prepared from 5-formyl-2-(2-fluoro-6-methoxy-phenoxy)-aniline (261 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-52abff3324184693b96f007167eeb75e
Source noteuspto-grants-2011_03