戻る
化工社化工社 化学情報印刷レポート · 研究参考用
HRID 131853作成日:2026年10月27日

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

https://huagongshe.com/reaction/131853

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1-Fluoro-2-nitrobenzeneHCID 73895—
反応物CyclopentanemethanolHCID 77195—
反応物2-(Cyclopentylmethoxy)anilineHCID 19754712—
生成物N-[2-(Cyclopentylmethoxy)phenyl]-N'-(thiazol-2-yl)ureaHCID 5973272060%
生成物2-(Cyclopentylmethoxy)-1-nitrobenzeneHCID 6699890480%

反応手順

2-(Cyclopentylmethoxy)-1-nitrobenzene (443 mg, 80%) was prepared from cyclopentanemethanol (0.32 ml, 3.0 mmol) and 1-fluoro-2-nitrobenzene (0.36 g, 2.5 mmol) following the general procedure G. This was reduced to 2-(cyclopentylmethoxy)aniline (268 mg, 70%) following general procedure B. N-[2-(Cyclopentylmethoxy)phenyl]-N′-(thiazol-2-yl)urea (286 mg, 60%) was prepared from 2-(cyclopentylmethoxy)aniline (0.25 g, 1.5 mmol) and 2-aminothiazole (150 mg, 1.5 mmol) following the general procedure D.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07384967B2
出典データセットuspto-grants-2008_06
ORD IDord-92b0c447208c44e08a1489467c195453
出典メモuspto-grants-2008_06