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HRID 391510作成日:2026年10月26日

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

https://huagongshe.com/reaction/391510

反応式

関与物質

役割名称HCID仕込み量
反応物1,1'-CarbonyldiimidazoleHCID 68263—
反応物5-(2-Phenyleth-1-Ynyl)Nicotinic AcidHCID 2779236—
反応物(S)-(+)-S-Methyl-S-phenylsulfoximineHCID 25036288—
溶媒TetrahydrofuranHCID 8028—
生成物N-[methyl(oxo)phenyl-lambda6-sulfanylidene]-5-(phenylethynyl)nicotinamideHCID 282240556%

反応条件

温度50 °C

反応手順

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%).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08383825B2
出典データセットuspto-grants-2013_02
ORD IDord-b6735c799eee440db8eae84f1f4af96f
出典メモuspto-grants-2013_02