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HRID 2190362생성일: 2026년 10월 25일

1-Fluoro-3-nitrobenzene → N-[6-(3-nitrophenoxy)-1,3-benzothiazol-2-yl]cyclopropanecarboxamide

https://huagongshe.com/reaction/2190362

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참여 물질

역할이름HCID투입량
반응물1-Fluoro-3-nitrobenzeneHCID 9823—
반응물Potassium CarbonateHCID 11430—
반응물18-Crown-6HCID 28557—
반응물HCID 57980821HCID 57980821—
용매DimethylformamideHCID 6228—
용매HexaneHCID 8058—
용매Ethyl AcetateHCID 8857—
생성물N-[6-(3-nitrophenoxy)-1,3-benzothiazol-2-yl]cyclopropanecarboxamideHCID 5774925636.2%

반응 조건

온도150 °C

반응 단계

To a suspension of N-(6-hydroxy-1,3-benzothiazol-2-yl)cyclopropanecarboxamide (1.53 g, 6.53 mmol) and potassium carbonate (3.72 g, 26.9 mmol) in N,N-dimethylformamide (50 mL) were added 1-fluoro-3-nitrobenzene (1.08 g, 7.65 mmol) and 18-crown-6 (1.07 g, 4.05 mmol), and the mixture was stirred at 150° C. for 14 hr. The reaction mixture was cooled to room temperature, and added to a mixed solvent (1:1, 300 mL) of ethyl acetate and hexane. The mixture was washed with water (200 mL) and saturated brine (200 mL), successively, and dried over anhydrous magnesium sulfate. The insoluble material was collected by filtration, and the residue was subjected to silica gel column chromatography using ethyl acetate and hexane (1:1) as an eluent to give the title compound (840 mg, 36%) as a pale-yellow solid.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08324395B2
출처 데이터셋uspto-grants-2012_12
ORD IDord-4623aad3604e4a868fe547e92e5bc920
출처 메모uspto-grants-2012_12