戻る
化工社化工社 化学情報印刷レポート · 研究参考用
HRID 599072作成日:2026年10月24日

2-Aminothiazole → 4-Fluoro-2-(2-methylsulfanylphenoxy)-1-nitrobenzene

https://huagongshe.com/ja/reaction/599072

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2,5-DifluoronitrobenzeneHCID 67767—
反応物4-Fluoro-2-(2-methylsulfanylphenoxy)anilineHCID 63649305—
生成物1-[4-Fluoro-2-(2-methylsulfanyl-phenoxy)-phenyl]-3-thiazol-2-yl-ureaHCID 5771237960%
生成物4-Fluoro-2-(2-methylsulfanylphenoxy)-1-nitrobenzeneHCID 6699915268%

反応手順

4-Fluoro-2-(2-methylsulfanylphenoxy)-1-nitrobenzene (1.06 g, 68%) was prepared from 2-hydroxythioanisole (0.77 g, 5.5 mmol) and 2,5-difluoro-1-nitro-benzene (0.80 g, 5.0 mmol) following the general procedure A. This was reduced to 4-fluoro-2-(2-methanesulfanyl-phenoxy)-phenylamine (0.52 g, 62%) following general procedure C. 1-[4-Fluoro-2-(2-methylsulfanyl-phenoxy)-phenyl]-3-thiazol-2-yl-urea (117 mg, 60%) was prepared from 4-fluoro-2-(2-methylsulfanylphenoxy)aniline (125 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US07897628B2
出典データセットuspto-grants-2011_03
ORD IDord-7a3a575f698f454e85b352a902420161
出典メモuspto-grants-2011_03