戻る
化工社化工社 化学情報印刷レポート · 研究参考用
HRID 1859753作成日:2026年10月27日

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

https://huagongshe.com/reaction/1859753

反応式

関与物質

役割名称HCID仕込み量
反応物Lawesson's reagentHCID 87949—
反応物3-(3,5-Dichloro-benzenesulfonylamino)-4-methoxy-N-phenyl-benzamideHCID 9890016—
溶媒TetrahydrofuranHCID 8028—
生成物3-(3,5-Dichloro-benzenesulfonylamino)-4-methoxy-N-phenyl-thiobenzamideHCID 993427281.8%

反応条件

温度50 °C

反応手順

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.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US06528528B2
出典データセットuspto-grants-2003_03
ORD IDord-834a1716c6a84ec99a7275aab0382cf6
出典メモuspto-grants-2003_03