HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 391510Erstellt: 24. Oktober 2026
1,1'-Carbonyldiimidazole → N-[methyl(oxo)phenyl-lambda6-sulfanylidene]-5-(phenylethynyl)nicotinamide
https://huagongshe.com/de/reaction/391510
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | 1,1'-Carbonyldiimidazole | HCID 68263 | — |
| Edukt | 5-(2-Phenyleth-1-Ynyl)Nicotinic Acid | HCID 2779236 | — |
| Edukt | (S)-(+)-S-Methyl-S-phenylsulfoximine | HCID 25036288 | — |
| Lösungsmittel | Tetrahydrofuran | HCID 8028 | — |
| Produkt | N-[methyl(oxo)phenyl-lambda6-sulfanylidene]-5-(phenylethynyl)nicotinamide | HCID 2822405 | 56% |
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-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%).
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patentnummer | US08383825B2 |
|---|
| Quelldatensatz | uspto-grants-2013_02 |
|---|
| ORD ID | ord-b6735c799eee440db8eae84f1f4af96f |
|---|
| Quellennotiz | uspto-grants-2013_02 |
|---|