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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 222256생성일: 2026년 10월 26일

Pyridine → S-(4-methylphenyl) 2-methyl-5-phenylpyridine-3-carbothioate

https://huagongshe.com/reaction/222256

반응식

참여 물질

역할이름HCID투입량
반응물PyridineHCID 1049—
반응물4-MethylbenzenethiolHCID 7811—
반응물Oxalyl chlorideHCID 65578—
반응물2-Methyl-5-phenylnicotinic acidHCID 57900081—
촉매4-(Dimethylamino)pyridineHCID 14284—
용매DichloromethaneHCID 6344—
용매Ethyl AcetateHCID 8857—
생성물S-(4-methylphenyl) 2-methyl-5-phenylpyridine-3-carbothioateHCID 57722887—

반응 조건

온도40 °C

반응 단계

To a 0° C. solution of 2-methyl-5-phenylnicotinic acid (100 mg, 0.40 mmol) in CH2Cl2 (4 mL) was added oxalyl chloride (344 μL, 4.0 mmol). The mixture was stirred at 40° C. After 3 hours, the mixture was concentrated to dryness, dissolved in benzene (2×5 mL) and concentrated again. After dissolving the crude residue in CH2Cl2 (2 mL) at 0° C., pyridine (1 mL, 0.92 M in CH2Cl2), 4-dimethylaminopyridine (10 mg, 0.08 mmol) and 4-methylthiophenol (60 mg, 0.48 mmol) were added. The mixture was then allowed to warm to room temperature. After stirring for 2 hours, the mixture was diluted with EtOAc, washed with 1N HCl, brine, dried over sodium sulfate, filtered, and concentrated. The crude residue was purified by flash chromatography (100-80% hexanes/EtOAc gradient) to afford the title compound. LRMS (APCI) calculated for C20H18NOS [M+H]+, 320.1; found 320.1.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08207186B2
출처 데이터셋uspto-grants-2012_06
ORD IDord-e2118e95ddae4cefaff1e41765265bbe
출처 메모uspto-grants-2012_06