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HRID 1356869作成日:2026年10月27日

Phenylalanine amide → N-(toluene-4-sulfonyl)-L-prolyl-L-phenylalanine amide

https://huagongshe.com/reaction/1356869

反応式

関与物質

役割名称HCID仕込み量
反応物Phenylalanine amideHCID 445694—
反応物(2S)-1-(4-methylbenzenesulfonyl)pyrrolidine-2-carboxylic acidHCID 691957—
生成物N-(toluene-4-sulfonyl)-L-prolyl-L-phenylalanine amideHCID 54382446—

反応手順

N-(Toluene-4-sulfonyl)-L-proline was reacted with L-phenylalanine amide using the procedure described in Method 12 to yield N-(toluene-4-sulfonyl)-L-prolyl-L-phenylalanine amide. To a solution of NaH (60% mineral oil—prewashed with THF) in THF at 0° C. was added N-(toluene-4-sulfonyl)-L-prolyl-L-phenylalanine amide and the reaction was stirred at 0° C. for 45 minutes. Toluene-4-sulfonyl chloride was added and the reaction was stirred for 16 hours at room temperature. The reaction mixture was extracted with EtOAc (3×50 mL) and 0.2 N HCl (50 mL), and the combined organic layers were washed successively with sat. NaHCO (50 mL), and sat. NaCl (2×50 mL), dried over MgSO4, filtered, and concentrated to yield the title compound as an oil.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US06586602B2
出典データセットuspto-grants-2003_07
ORD IDord-cba6a8fa5756421ea6f9e46fab4dc483
出典メモuspto-grants-2003_07