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HRID 8639作成日:2026年10月23日

4-Toluenesulfonyl chloride → Toluene-4-sulfonic acid 2-[tert-butoxycarbonyl-(3-fluoro-benzyl)-amino]-ethyl ester

https://huagongshe.com/ja/reaction/8639

反応式

関与物質

役割名称HCID仕込み量
反応物4-Toluenesulfonyl chlorideHCID 7397—
反応物TriethylamineHCID 8471—
反応物2-(3-Fluoro-benzylamino)-ethanolHCID 10866749—
反応物tert-butyl N-[(3-fluorophenyl)methyl]-N-(2-hydroxyethyl)carbamateHCID 69653122—
溶媒DichloromethaneHCID 6344—
生成物Toluene-4-sulfonic acid 2-[tert-butoxycarbonyl-(3-fluoro-benzyl)-amino]-ethyl esterHCID 23548235—

反応手順

Add p-toluenesulfonyl-chloride (0.71 g, 3.71 mmol), portionwise, to a mixture of (3-fluoro-benzyl)-(2-hydroxy-ethyl)-carbamic acid dimethyl-ethyl ester (1 g, 3.71 mmol, prepared from 2-(3-fluoro-benzylamino)-ethanol by methods as are known in the art), triethylamine (0.751 g, 7.4 mmol) and dichloromethane (6 mL). Stir the resulting suspension vigorously overnight at room temperature. Add water (10 mL), separate the organic layer, and extract the aqueous layer with dichloromethane (5 mL), twice. Combine the organic layers and wash with citric acid (5 mL, 20% in water), dry with sodium sulfate and evaporate the solvent to give the final, desired compound. The final compound may be purified by chromatography.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07091199B1
出典データセットuspto-grants-2006_08
ORD IDord-3bfb9478b47f4e919a8a0e2f00a8190d
出典メモuspto-grants-2006_08