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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1672605Erstellt: 26. Oktober 2026

Trifluoromethanesulfonic acid → 5-Iodo-6-methyl-N-[4-(methylsulfonyl)benzyl]-2-oxo-1-[3-(trifluoro-methyl)phenyl]1,2-dihydropyridine-3-carboxamide

https://huagongshe.com/reaction/1672605

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktTrifluoromethanesulfonic acidHCID 62406—
EduktN-IodosuccinimideHCID 120273—
Edukt6-methyl-N-[4-(methylsulfonyl)benzyl]-2-oxo-1-[3-(trifluoromethyl)phenyl]-1,2-dihydropyridine-3-carboxamideHCID 11619625—
LösungsmittelAcetonitrileHCID 6342—
LösungsmittelDichloromethaneHCID 6344—
Produkt5-Iodo-6-methyl-N-[4-(methylsulfonyl)benzyl]-2-oxo-1-[3-(trifluoro-methyl)phenyl]1,2-dihydropyridine-3-carboxamideHCID 11519933—

Reaktionsschritte

To a solution of 6-methyl-N-[4-(methylsulfonyl)benzyl]-2-oxo-1-[3-(trifluoromethyl)phenyl]-1,2-dihydropyridine-3-carboxamide (200 mg, 0.43 mmol) in MeCN (1.5 ml) at RT and under argon, was added trifluoromethanesulfonic acid (1 ml) followed by N-iodosuccinimide (97 mg, 0.43 mmol). After 45 min, the reaction mixture was diluted with DCM, washed with aqueous NaHCO3, with aqueous NaS2O4 and water, dried (Na2SO4), and evaporated to give the title compound SM1 (200 mg).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07998984B2
Quelldatensatzuspto-grants-2011_08
ORD IDord-0c86cee69a13425b833bed6b281f2ba3
Quellennotizuspto-grants-2011_08