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HRID 559854作成日:2026年10月25日

2-Aminothiazole → 2-(2-Methylsulfanylphenoxy)-1-nitrobenzene

https://huagongshe.com/reaction/559854

反応式

関与物質

役割名称HCID仕込み量
反応物2-AminothiazoleHCID 2155—
反応物o-(Methylthio)phenolHCID 61261—
反応物1-Fluoro-2-nitrobenzeneHCID 73895—
反応物2-(2-Methylsulfanylphenoxy)anilineHCID 59783707—
生成物N-[2-(2-Methylsulfanylphenoxy)phenyl]-N'-(thiazol-2-yl)ureaHCID 5973270165%
生成物2-(2-Methylsulfanylphenoxy)-1-nitrobenzeneHCID 5978361568%

反応手順

2-(2-Methylsulfanylphenoxy)-1-nitrobenzene (0.88 g, 68%) was prepared from 2-hydroxythioanisole (0.77 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-(2-methylsulfanylphenoxy)aniline (0.53 g, 68%) following general procedure B. N-[2-(2-Methylsulfanylphenoxy)phenyl]-N′-(thiazol-2-yl)urea (115 mg, 65%) was prepared from 2-(2-methylsulfanylphenoxy)aniline (115 mg, 0.5 mmol) and 2-aminothiazole (60 mg, 0.6 mmol) following the general procedure D.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08063081B2
出典データセットuspto-grants-2011_11
ORD IDord-b67649e84346464db1e1ac55f192b8e4
出典メモuspto-grants-2011_11