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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 391510생성일: 2026년 10월 24일

1,1'-Carbonyldiimidazole → N-[methyl(oxo)phenyl-lambda6-sulfanylidene]-5-(phenylethynyl)nicotinamide

https://huagongshe.com/reaction/391510

반응식

참여 물질

역할이름HCID투입량
반응물1,1'-CarbonyldiimidazoleHCID 68263—
반응물5-(2-Phenyleth-1-Ynyl)Nicotinic AcidHCID 2779236—
반응물(S)-(+)-S-Methyl-S-phenylsulfoximineHCID 25036288—
용매TetrahydrofuranHCID 8028—
생성물N-[methyl(oxo)phenyl-lambda6-sulfanylidene]-5-(phenylethynyl)nicotinamideHCID 282240556%

반응 조건

온도50 °C

반응 단계

To a slurry of 5-(2-phenyleth-1-ynyl)nicotinic acid (339 mg, 1.5 mmol) in 6.0 mL THF at room temperature was added 1,1′-carbonyldiimidazole (271 mg, 1.7 mmol). After stirring 1.25 hour, a solution of (S)-(+)-S-methyl-S-phenylsulfoximine (260 mg, 1.7 mmol) in 1.5 mL THF was added and the mixture heated at 50° C. for 22 hours. Then an additional 50 mg (0.32 mmol) (S)-(+)-S-methyl-S-phenylsulfoximine was added and heating continued at 60° C. for 3.5 hours. The reaction was quenched with NaHCO3 solution and then extracted into EtOAc. The EtOAc layer was washed with NaHCO3 solution, H2O, brine, dried with anhydrous Na2SO4 and concentrated. The yellow oil obtained was chromatographed eluting with hexane/EtOAc to give N-[methyl(oxo)phenyl-λ6-sulfanylidene]-5-(phenylethynyl)nicotinamide as a white foam (303 mg, 55%).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08383825B2
출처 데이터셋uspto-grants-2013_02
ORD IDord-b6735c799eee440db8eae84f1f4af96f
출처 메모uspto-grants-2013_02