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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1387596Erstellt: 26. Oktober 2026

Lawesson's reagent → 3-(3,5-Dichloro-benzenesulfonylamino)-4-methoxy-N-phenyl-thiobenzamide

https://huagongshe.com/reaction/1387596

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktLawesson's reagentHCID 87949—
Edukt3-(3,5-Dichloro-benzenesulfonylamino)-4-methoxy-N-phenyl-benzamideHCID 9890016—
LösungsmittelTetrahydrofuranHCID 8028—
Produkt3-(3,5-Dichloro-benzenesulfonylamino)-4-methoxy-N-phenyl-thiobenzamideHCID 993427281,8%

Reaktionsbedingungen

Temperatur50 °C

Reaktionsschritte

A mixture of 3-(3,5-dichloro-benzenesulfonylamino)-4-methoxy-N-phenyl-benzamide from Example 118 (3.61 g, 8.0 mmol) and Lawesson's reagent (3.57 g, 8.8 mmol) was stirred at room temperature overnight in tetrahydrofuran (250 mL). The reaction mixture was warmed to 50° C. for about one hour, then to 65° C. for about 4 hours then stirred at room temperature overnight. The mixture was concentrated to dryness and the residue dissolved in ethyl acetate and filtered through silica gel. Concentration of the eluant followed by trituration in hexanes/ethyl acetate (1:1) afforded the crude product (3.06 g). A portion (0.8 g) of this was chromatographed on silica gel in hexanes/ethyl acetate (1:1) to afford a pure sample (0.324 g); m.p. 206-208° C.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS06268387B1
Quelldatensatzuspto-grants-2001_07
ORD IDord-a1c4d9bf5c8647c4802bdc219ee282bc
Quellennotizuspto-grants-2001_07