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HRID 1243271作成日:2026年10月27日

phenylalaninol, (S)- → N-{(S)-1-hydroxy-3-phenyl-2-propyl}-5-benzyloxy-2-hydroxybenzamide

https://huagongshe.com/reaction/1243271

反応式

関与物質

役割名称HCID仕込み量
反応物phenylalaninol, (S)-HCID 447213—
反応物Methyl 5-(benzyloxy)-2-hydroxybenzoateHCID 13026913—
溶媒DimethylformamideHCID 6228—
溶媒HexaneHCID 8058—
溶媒Ethyl AcetateHCID 8857—
生成物N-{(S)-1-hydroxy-3-phenyl-2-propyl}-5-benzyloxy-2-hydroxybenzamideHCID 1775179550%

反応手順

In a flask equipped with a reflux condenser and a magnetic stirring bar are dissolved the methyl 5-benzyloxy-2-hydroxybenzoate and one equivalent of 2-(S)-amino-3-phenyl-1-propanol in dry dimethyl formamide. The flask is immersed in an oil bath at 75° C. and left to stir for 72 hours. The solvent is evaporated and the residue is isolated through the use of a silica gel column using a mixture of ethyl acetate and hexane as eluent. In this fashion is obtained in 50% yield, N-{(S)-1-hydroxy-3-phenyl-2-propyl}-5-benzyloxy-2-hydroxybenzamide.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07119068B2
出典データセットuspto-grants-2006_10
ORD IDord-e69800c873b74ff8b817a59654fbcfe9
出典メモuspto-grants-2006_10