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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 336906Erstellt: 24. Oktober 2026

(Methoxycarbonylsulfamoyl)triethylammonium hydroxide → HCID 66602141, Verbindung

https://huagongshe.com/de/reaction/336906

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Edukt(Methoxycarbonylsulfamoyl)triethylammonium hydroxideHCID 11032497—
EduktHCID 58133772HCID 58133772—
LösungsmittelTetrahydrofuranHCID 8028—
LösungsmittelEthyl AcetateHCID 8857—
ProduktHCID 66602141HCID 66602141—

Reaktionsschritte

The reaction was carried out under argon. (rac)-4-{2-[(2-{[tert-Butyl(dimethyl)silyl]oxy}ethyl)sulfonyl]-4-cyanophenyl}-6-methyl-2-oxo-1-[3-(trifluoromethyl)phenyl]-1,2,3,4-tetrahydropyrimidine-5-carboxamide (740 mg, 1.18 mmol) was initially charged in dry THF (30 ml), methoxycarbonylsulfamoyltriethylammonium hydroxide (Burgess reagent; 1.699 g, 7.13 mmol; 6 eq.) was added and the mixture was stirred at RT. After 75 min, HPLC control showed complete conversion. The reaction mixture was then taken up in ethyl acetate (150 ml). The organic phase was washed with saturated sodium chloride solution (3×50 ml), dried over solid sodium sulfate, filtered and concentrated. The residue was subjected to flash chromatography on silica gel (mobile phase: cyclohexane/ethyl acetate 1:1). The title compound was obtained as a colorless solid (550 mg, 77% of theory).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08889700B2
Quelldatensatzuspto-grants-2014_11
ORD IDord-4e2d787ee2cf446c8b76123e5fd73696
Quellennotizuspto-grants-2014_11