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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1896681생성일: 2026년 10월 27일

Ethyl Acetate → N-(4-Chlorophenyl)-2-[2-(4-pyridyl)ethylthio]pyridine-3-carboxamide

https://huagongshe.com/reaction/1896681

반응식

참여 물질

역할이름HCID투입량
반응물Ethyl AcetateHCID 8857—
반응물Sodium hydrideHCID 24758—
반응물4-PyridoethanethiolHCID 150969—
반응물2-chloro-N-(4-chlorophenyl)pyridine-3-carboxamideHCID 587906—
용매DimethylformamideHCID 6228—
생성물N-(4-Chlorophenyl)-2-[2-(4-pyridyl)ethylthio]pyridine-3-carboxamideHCID 5294856488%

반응 단계

To a suspension of 60% sodium hydride (35 mg, 0.88 mmol) in N,N-dimethylformamide (1 mL), a solution of 4-pyridineethanethiol (104 mg, 0.75 mmol) in N,N-dimethylformamide (1.5 mL) and a solution of 2-chloro-N-(4-chlorophenyl)pyridine-3-carboxamide (200 mg, 0.75 mmol, Reference compound No. 2-1) in N,N-dimethylformamide (1.5 mL) were added under ice-cooling successively. The reaction mixture was stirred at room temperature for 2 hours, and then ethyl acetate (40 mL) was added thereto. The ethyl acetate layer was washed with water (40 mL) and brine (40 mL) and dried over anhydrous magnesium sulfate, then the solvent was evaporated under reduced pressure. The precipitated solid was filtered off and washed with diethyl ether:ethyl acetate (3:1). The solid was dried under reduced pressure to give 240 mg of the target compound as a white solid. (Yield 88%)

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08518973B2
출처 데이터셋uspto-grants-2013_08
ORD IDord-06d4bc38b4774d249017c38d9cc85aaf
출처 메모uspto-grants-2013_08