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HRID 1351791作成日:2026年10月25日

Hydrochloric Acid → 3-[[2-(2-Tert-butylsulfamoyl-4-isopropylphenyl)ethyl]sulfamoyl]-4-methoxybenzamide

https://huagongshe.com/reaction/1351791

反応式

関与物質

役割名称HCID仕込み量
反応物Hydrochloric AcidHCID 313—
反応物TriethylamineHCID 8471—
反応物5-Carbamoyl-2-methoxybenzenesulfonyl chlorideHCID 15922008—
反応物2-(2-aminoethyl)-N-tert-butyl-5-isopropylbenzenesulfonamideHCID 17856312—
溶媒WaterHCID 962—
溶媒DimethylformamideHCID 6228—
生成物3-[[2-(2-Tert-butylsulfamoyl-4-isopropylphenyl)ethyl]sulfamoyl]-4-methoxybenzamideHCID 1845694586.3%

反応手順

To a suspension of 241 mg of 5-carbamoyl-2-methoxybenzenesulfonyl chloride and 288 mg of 2-(2-aminoethyl)-N-tert-butyl-5-isopropylbenzenesulfonamide in 10 mL of N,N-dimethylformamide was added 0.32 mL of triethylamine, and the mixture was stirred at room temperature for 3 days. To the reaction mixture was added 30 mL of water, and the mixture was stirred at the same temperature for 1 hour. To the mixture was added 10 mL of 1 mol/L hydrochloric acid, and the mixture was extracted three times with 20 mL of ethyl acetate. The organic layers were combined and washed with 30 mL of water, and dried over anhydrous magnesium sulfate. The solvent was removed under reduced pressure to give 426 mg of 3-[[2-(2-tert-butylsulfamoyl-4-isopropylpheyl)ethyl]sulfamoyl]-4-methoxybenzamide.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07217832B2
出典データセットuspto-grants-2007_05
ORD IDord-492aed558a3f4446a20785ebe4fe4cb3
出典メモuspto-grants-2007_05