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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1859753Generated: October 26, 2026

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

https://huagongshe.com/reaction/1859753

Reaction equation

Participants

RoleNameHCIDCharge
ReactantLawesson's reagentHCID 87949—
Reactant3-(3,5-Dichloro-benzenesulfonylamino)-4-methoxy-N-phenyl-benzamideHCID 9890016—
SolventTetrahydrofuranHCID 8028—
Product3-(3,5-Dichloro-benzenesulfonylamino)-4-methoxy-N-phenyl-thiobenzamideHCID 993427281.8%

Reaction Conditions

Temperature50 °C

Reaction Steps

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 tetrahydro-furan (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.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06528528B2
Source datasetuspto-grants-2003_03
ORD IDord-834a1716c6a84ec99a7275aab0382cf6
Source noteuspto-grants-2003_03