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HRID 926039作成日:2026年10月24日

Dichloromethane → HCID 71238589、化合物

https://huagongshe.com/ja/reaction/926039

反応式

関与物質

役割名称HCID仕込み量
反応物DichloromethaneHCID 6344—
反応物TriethylamineHCID 8471—
反応物Ethyl 1-aminocyclopropane-1-carboxylate hydrochlorideHCID 386203—
反応物2-(Trimethylsilyl)ethyl 3-(chlorosulfonyl)benzoateHCID 86676334—
溶媒PyridineHCID 1049—
生成物HCID 71238589HCID 7123858993.1%

反応手順

A mixture of 774 mg of ethyl 1-aminocyclopropane-1-carboxylate hydrochloride, 1.4 mL of triethylamine, and 15 mL of dichloromethane was stirred at room temperature for 30 minutes, and 15 mL of pyridine and 1.50 g of 2-(trimethylsilyl)ethyl 3-(chlorosulfonyl)benzoate were added thereto in this order, followed by stirring at room temperature overnight. The reaction mixture was concentrated under reduced pressure, and to the residue was added an aqueous citric acid solution, followed by extraction with ethyl acetate. The organic layer was washed with saturated brine, then dried over anhydrous sodium sulfate, and concentrated under reduced pressure. The obtained residue was purified by silica gel column chromatography (hexane-ethyl acetate) to obtain 1.80 g of 2-(trimethylsilyl)ethyl 3-{[1-(ethoxycarbonyl)cyclopropyl]sulfamoyl}benzoate as a pale yellow oily substance.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US09284295B2
出典データセットuspto-grants-2016_03
ORD IDord-3341629265ae48ab83f525048cdd5e8a
出典メモuspto-grants-2016_03