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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1983232생성일: 2026년 10월 23일

2-Aminothiazole → 1-(4-Fluorophenoxy)-2-nitrobenzene

https://huagongshe.com/ko/reaction/1983232

반응식

참여 물질

역할이름HCID투입량
반응물2-AminothiazoleHCID 2155—
반응물4-FluorophenolHCID 9732—
반응물1-Fluoro-2-nitrobenzeneHCID 73895—
반응물2-(4-Fluorophenoxy)anilineHCID 6485399—
생성물1-(4-Fluorophenoxy)-2-nitrobenzeneHCID 96112775%
생성물N-[2-(4-Fluorophenoxy)phenyl]-N'-(thiazol-2-yl)ureaHCID 5973293772%

반응 단계

2-(4-Fluorophenoxy)-1-nitrobenzene (0.87 g, 75%) was prepared from 4-fluoro-phenol (0.62 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-(4-fluorophenoxy)aniline (0.51 g, 68%) following general procedure B. N-[2-(4-Fluorophenoxy)phenyl]-N′-(thiazol-2-yl)urea (118 mg, 72%) was prepared from 2-(4-fluorophenoxy)aniline (102 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 번호US07541373B2
출처 데이터셋uspto-grants-2009_06
ORD IDord-203f80ffd9ff4fd795236569ea5e8d6a
출처 메모uspto-grants-2009_06