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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 131844생성일: 2026년 10월 26일

2-Aminothiazole → Benzene, 1-fluoro-2-[(2-nitrophenyl)thio]-

https://huagongshe.com/reaction/131844

반응식

참여 물질

역할이름HCID투입량
반응물2-AminothiazoleHCID 2155—
반응물1-Fluoro-2-nitrobenzeneHCID 73895—
반응물2-FluorothiophenolHCID 520216—
반응물2-(2-Fluorophenylsulfanyl)anilineHCID 11850357—
생성물Benzene, 1-fluoro-2-[(2-nitrophenyl)thio]-HCID 1185028783%
생성물HCID 59733001HCID 5973300175%

반응 단계

2-(2-Fluorophenylsulfanyl)nitrobenzene (1.03 g, 83%) was prepared from 2-fluorothiophenol (0.70 g, 5.5 mmol) and 2-fluoronitrobenzene (0.71 g, 5.0 mmol) following the general procedure A. This compound was reduced to 2-(2-fluorophenylsulfanyl)aniline (0.65 g, 72%) following general procedure B. N-[2-(2-Fluorophenylsulfanyl)phenyl]-N′-(thiazol-2-yl)urea (129 mg, 75%) was prepared from 2-(2-fluorophenylsulfanyl)aniline (107 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-782ed4d5a4c34964901422f06cd6ca0d
출처 메모uspto-grants-2008_06