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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 493237생성일: 2026년 10월 26일

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

https://huagongshe.com/reaction/493237

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 번호US07534802B2
출처 데이터셋uspto-grants-2009_05
ORD IDord-3513bcd552b642419c961cb32ff7f47f
출처 메모uspto-grants-2009_05