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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2276100Generated: October 25, 2026

2-Aminothiazole → N-[2-(4-Methoxy-2-methoxycarbonylphenoxy)phenyl]-N'-(thiazol-2-yl)urea

https://huagongshe.com/reaction/2276100

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-AminothiazoleHCID 2155—
Reactant1-Fluoro-2-nitrobenzeneHCID 73895—
ReactantMethyl 2-hydroxy-5-methoxybenzoateHCID 4072341—
Reactant2-[4-Methoxy-2-(methoxycarbonyl)phenoxy]anilineHCID 59783886—
ProductN-[2-(4-Methoxy-2-methoxycarbonylphenoxy)phenyl]-N'-(thiazol-2-yl)ureaHCID 5973283166%
Product2-[4-Methoxy-2-methoxycarbonylphenoxy]-1-nitrobenzeneHCID 5978386152%

Reaction Steps

2-[4-Methoxy-2-methoxycarbonylphenoxy]-1-nitrobenzene (0.78 g, 52%) was prepared from methyl 5-methoxysalicylate (1.0 g, 5.5 mmol) and 1-fluoro-2-nitrobenzene (0.71 g, 5.0 mmol) following the general procedure A. This was reduced to 2-[4-methoxy-2-(methoxycarbonyl)phenoxy]aniline (0.47 g, 68%) following general procedure B. N-[2-(4-Methoxy-2-methoxycarbonylphenoxy)phenyl]-N′-(thiazol-2-yl)urea (130 mg, 66%) was prepared from 2-[4-methoxy-2-(methoxycarbonyl)phenoxy]aniline (136 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 numberUSRE045670E1
Source datasetuspto-grants-2015_09
ORD IDord-77d0d2d5404146a2acfc34a00d3b350a
Source noteuspto-grants-2015_09