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HRID 30901생성일: 2026년 10월 23일

4-Bromo-2-fluoroaniline → N-(4-bromo-2-fluorophenyl)-N-(6-trifluoromethoxy-1,3-benzothiazol-2-yl)amine

https://huagongshe.com/ko/reaction/30901

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참여 물질

역할이름HCID투입량
반응물4-Bromo-2-fluoroanilineHCID 123050—
반응물2-Chloro-6-(trifluoromethoxy)-1,3-benzothiazoleHCID 10037924—
용매1-ButanolHCID 263—
용매1,4-DioxaneHCID 31275—
생성물N-(4-bromo-2-fluorophenyl)-N-(6-trifluoromethoxy-1,3-benzothiazol-2-yl)amineHCID 2198577858.1%

반응 조건

온도90 °C

반응 단계

In a 250-mL round-bottom flask, 2-chloro-6-trifluoromethoxy-1,3-benzothiazole (5.36 g, 21.14 mmol) and 4-bromo-2-fluoroaniline (4.82 g, 25.36 mmol) were combined in 100 mL n-butanol containing 1% 4.0 M HCl in dioxane, and heated at 90° C. overnight. The mixture was cooled to rt and the solvent was removed under reduced pressure. Ethyl acetate (50 mL) was added, and the mixture was ultrasonicated by suspending the flask in an ultrasonication bath for 30 minutes. The mixture was filtered, and the filtrate was concentrated under reduced pressure. Acetonitrile (50 mL) was added to the mixture, which was then ultrasonicated for 30 minutes and then filtered to provide the product as a white solid (5 g, 58%). LC-MS m/z 409.1 (MH+), ret. time 4.02 min.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07423156B2
출처 데이터셋uspto-grants-2008_09
ORD IDord-90ba5aab8e7741e6b17339b8382e4634
출처 메모uspto-grants-2008_09