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HRID 999作成日:2026年10月24日

Ethyl isothiocyanatoformate → N-tert-butyl-5-[N-(ethoxycarbonylaminothiocarbonyl)methylamino]-2-methoxycarbonylbenzenesulfonamide

https://huagongshe.com/ja/reaction/999

反応式

関与物質

役割名称HCID仕込み量
反応物Ethyl isothiocyanatoformateHCID 85320—
反応物N-tert-Butyl-2-methoxycarbonyl-5-methylaminobenzenesulfonamideHCID 19693799—
溶媒DimethylformamideHCID 6228—
溶媒Ethyl AcetateHCID 8857—
生成物N-tert-butyl-5-[N-(ethoxycarbonylaminothiocarbonyl)methylamino]-2-methoxycarbonylbenzenesulfonamideHCID 5417042075%

反応手順

1.20 g (4.0 mmol) of N-tert-butyl-2-methoxycarbonyl-5-methylaminobenzenesulfonamide is dissolved in 5 ml of anhydrous DMF, and 0.60 g (4.3 mmol) of 95% strength ethoxycarbonyl isothiocyanate is added. After 3 h at room temperature the mixture is taken up in ethyl acetate and washed with 1N hydrochloric acid and water. The organic phase is dried over magnesium sulfate and the solvent is removed by distillation. The residue is taken up in a little ethyl acetate and precipitated with heptane at -25° C. The precipitate is filtered off with suction and dried to give 1.29 g (75% of theory) of colorless N-tert-butyl-5-[N-(ethoxycarbonylaminothiocarbonyl)methylamino]-2-methoxycarbonylbenzenesulfonamide. m.p.: 110° C.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05723409
出典データセットuspto-grants-1998_03
ORD IDord-eb3a2bf3a97a4cecad374cf323a11215
出典メモuspto-grants-1998_03