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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 607348Erstellt: 25. Oktober 2026

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

https://huagongshe.com/reaction/607348

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Edukt1,1'-CarbonyldiimidazoleHCID 68263—
Edukt5-(2-Phenyleth-1-Ynyl)Nicotinic AcidHCID 2779236—
Edukt(S)-(+)-S-Methyl-S-phenylsulfoximineHCID 25036288—
LösungsmittelTetrahydrofuranHCID 8028—
ProduktN-[methyl(oxo)phenyl-lambda6-sulfanylidene]-5-(phenylethynyl)nicotinamideHCID 2822405262,7%

Reaktionsbedingungen

Temperatur50 °C

Reaktionsschritte

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-5-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%).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07915443B2
Quelldatensatzuspto-grants-2011_03
ORD IDord-b9ffdc3b37ba45e898a0a7e5fb237601
Quellennotizuspto-grants-2011_03