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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 2272593생성일: 2026년 10월 27일

Water → 5-(3-chloro-4-cyanophenoxy)-N-(9-ethyl-9H-carbazol-3-yl)-3-hydroxy-3-methylpentanamide

https://huagongshe.com/reaction/2272593

반응식

참여 물질

역할이름HCID투입량
반응물WaterHCID 962—
반응물2-Chloro-4-fluorobenzonitrileHCID 109000—
반응물Potassium tert-butoxideHCID 23665647—
반응물N-(9-ethyl-9H-carbazol-3-yl)-3,5-dihydroxy-3-methylpentanamideHCID 86729751—
용매TetrahydrofuranHCID 8028—
생성물5-(3-chloro-4-cyanophenoxy)-N-(9-ethyl-9H-carbazol-3-yl)-3-hydroxy-3-methylpentanamideHCID 8672975248.6%

반응 단계

To a solution of the compound obtained in Step 1 (348 mg, 1.02 mmol) and 2-chloro-4-fluorobenzonitrile (159 mg, 1.02 mmol) in THF (10 mL) was added potassium t-butoxide (287 mg, 2.56 mmol), and the mixture was stirred at room temperature for 14 hr. Water was poured into the reaction mixture, and the mixture was extracted with ethyl acetate. The organic layer was washed with water and saturated brine, and dried, and the solvent was evaporated under reduced pressure. The obtained residue was purified by silica gel column chromatography (solvent gradient; 10 to 100% ethyl acetate/hexane) to give the title compound (236 mg, 0.496 mmol, 48.5%) as a white powder.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US09120776B2
출처 데이터셋uspto-grants-2015_09
ORD IDord-26ee037a40c04e91beb60a3cfdc1ab90
출처 메모uspto-grants-2015_09