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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 559893생성일: 2026년 10월 26일

2-Aminothiazole → 2-(2-Chloro-4-fluorophenylsulfanyl)nitrobenzene

https://huagongshe.com/reaction/559893

반응식

참여 물질

역할이름HCID투입량
반응물2-AminothiazoleHCID 2155—
반응물1-Fluoro-2-nitrobenzeneHCID 73895—
반응물2-Chloro-4-fluorothiophenolHCID 519446—
반응물2-(2-Chloro-4-fluorophenylsulfanyl)anilineHCID 66998238—
생성물N-[2-(2-Chloro-4-fluorophenylsulfanyl)phenyl]-N'-(thiazol-2-yl)ureaHCID 5973275276%
생성물2-(2-Chloro-4-fluorophenylsulfanyl)nitrobenzeneHCID 6699896080%

반응 단계

2-(2-Chloro-4-fluorophenylsulfanyl)nitrobenzene (1.13 g, 80%) was prepared from 2-chloro-4-fluorothiophenol (0.89 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-chloro-4-fluorophenylsulfanyl)aniline (0.76 g, 75%) following the general procedure B. N-[2-(2-Chloro-4-fluorophenylsulfanyl)phenyl]-N′-(thiazol-2-yl)urea (144 mg, 76%) was prepared from 2-(2-chloro-4-fluorophenylsulfanyl)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 번호US08063081B2
출처 데이터셋uspto-grants-2011_11
ORD IDord-971af2c9cacd4fd0a4b3534609928a70
출처 메모uspto-grants-2011_11