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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 2276145생성일: 2026년 10월 25일

2-Aminothiazole → 2-(2-Methoxyphenylsulfanyl)nitrobenzene

https://huagongshe.com/reaction/2276145

반응식

참여 물질

역할이름HCID투입량
반응물2-AminothiazoleHCID 2155—
반응물ThioguaiacolHCID 23642—
반응물1-Fluoro-2-nitrobenzeneHCID 73895—
반응물2-(2-Methoxyphenylsulfanyl)anilineHCID 20980631—
생성물2-(2-Methoxyphenylsulfanyl)nitrobenzeneHCID 82490782%
생성물N-[2-(2-Methoxyphenylsulfanyl)phenyl]-N'-(thiazol-2-yl)ureaHCID 5973308462%

반응 단계

2-(2-Methoxyphenylsulfanyl)nitrobenzene (1.07 g, 82%) was prepared from 2-methoxy thiophenol (0.76 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-methoxyphenylsulfanyl)aniline (0.66 g, 70%) following general procedure B. N-[2-(2-Methoxyphenylsulfanyl)phenyl]-N′-(thiazol-2-yl)urea (110 mg, 62%) was prepared from 2-(2-methoxyphenylsulfanyl)aniline (115 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 번호USRE045670E1
출처 데이터셋uspto-grants-2015_09
ORD IDord-8eda1d36f0034001a4f169ee9e459e6c
출처 메모uspto-grants-2015_09