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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1387596Generated: October 26, 2026

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

https://huagongshe.com/reaction/1387596

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 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.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06268387B1
Source datasetuspto-grants-2001_07
ORD IDord-a1c4d9bf5c8647c4802bdc219ee282bc
Source noteuspto-grants-2001_07