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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 131813Generated: October 24, 2026

2-Aminothiazole → 2-(3-Methoxy-2-methoxycarbonylphenoxy)-1-nitrobenzene

https://huagongshe.com/en/reaction/131813

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-AminothiazoleHCID 2155—
Reactant1-Fluoro-2-nitrobenzeneHCID 73895—
ReactantMethyl 2-hydroxy-6-methoxybenzoateHCID 527092—
Reactant2-(3-Methoxy-2-methoxycarbonylphenoxy)anilineHCID 66998871—
ProductN-[(3-methoxy-2-methoxycarbonylphenoxy)phenyl]-N'-(thiazol-2-yl)ureaHCID 5973282165%
Product2-(3-Methoxy-2-methoxycarbonylphenoxy)-1-nitrobenzeneHCID 6699883480%

Reaction Steps

2-(3-Methoxy-2-methoxycarbonylphenoxy)-1-nitrobenzene (1.21 g, 80%) was prepared from methyl 6-methoxysalicylate (1.09 g, 5.5 mmol) and 1-fluoro-2-nitrobenzene (0.71 g, 5.0 mmol) following the general procedure A. This compound was reduced to 2-(3-methoxy-2-methoxycarbonylphenoxy)aniline (0.82 g, 75%) following the general procedure C. N-[(3-methoxy-2-methoxycarbonylphenoxy)phenyl]-N′-(thiazol-2-yl)urea (130 mg, 65%) was prepared from 2-(3-methoxy-2-methoxycarbonylphenoxy)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 numberUS07384967B2
Source datasetuspto-grants-2008_06
ORD IDord-bfe7f4fbb7684d10bb8c292a558af4b0
Source noteuspto-grants-2008_06