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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 131821생성일: 2026년 10월 24일

2-Aminothiazole → 5-Fluoro-2-(2-fluoro-6-methoxyphenoxy)-1-nitrobenzene

https://huagongshe.com/ko/reaction/131821

반응식

참여 물질

역할이름HCID투입량
반응물2-AminothiazoleHCID 2155—
반응물2,5-DifluoronitrobenzeneHCID 67767—
반응물2-Fluoro-6-methoxyphenolHCID 2737367—
반응물5-Fluoro-2-(2-fluoro-6-methoxyphenoxy)anilineHCID 66998239—
생성물N-[5-Fluoro-2-(2-fluoro-6-methoxyphenoxy)phenyl]-N'-(thiazol-2-yl)ureaHCID 5973291169%
생성물5-Fluoro-2-(2-fluoro-6-methoxyphenoxy)-1-nitrobenzeneHCID 66998975539.3%

반응 단계

5-Fluoro-2-(2-fluoro-6-methoxyphenoxy)-1-nitrobenzene (0.91 g, 65%) was prepared from 2-fluoro-6-methoxyphenol (0.78 g, 5.5 mmol) and 2,5-difluoro-1-nitrobenzene (0.80 g, 5.0 mmol) following the general procedure A. This was reduced to 5-fluoro-2-(2-fluoro-6-methoxyphenoxy)aniline (0.66 g, 81%) following general procedure C. N-[5-Fluoro-2-(2-fluoro-6-methoxyphenoxy)phenyl]-N′-(thiazol-2-yl)urea (1309, 69%) was prepared from 5-fluoro-2-(2-fluoro-6-methoxyphenoxy)aniline (126 mg, 0.5 mmol) and 2-aminothiazole (60 mg, 0.6 mmol) following the general procedure D.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07384967B2
출처 데이터셋uspto-grants-2008_06
ORD IDord-867e53abdefb422fa7a085d135247e2b
출처 메모uspto-grants-2008_06