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HRID 322739作成日:2026年10月24日

Methyl 2-amino-3-(3-hydroxyphenyl)propanoate → Methyl N-[N-(3-nitrophenylacetyl)-L-alaninyl]-2-amino3-(3-hydroxyphenyl)propionate

https://huagongshe.com/ja/reaction/322739

反応式

関与物質

役割名称HCID仕込み量
反応物Methyl 2-amino-3-(3-hydroxyphenyl)propanoateHCID 22386100—
反応物N-(3-Nitrophenylacetyl)-L-alanineHCID 53788870—
溶媒Ethyl AcetateHCID 8857—
生成物Methyl N-[N-(3-nitrophenylacetyl)-L-alaninyl]-2-amino3-(3-hydroxyphenyl)propionateHCID 10159696—

反応手順

Following General Procedure C and using N-(3-nitrophenylacetyl)-L-alanine (prepared from 3-nitrophenylacetic acid (Aldrich) and L-alanine ethyl ester hydrochloride (Sigma) using General Procedure C, followed by hydrolysis using General Procedure AF) and methyl 2-amino-3-(3-hydroxyphenyl)propionate (prepared from 2-amino-3-(3-hydroxyphenyl)propionate (Biosynth AG, Switzerland) and methanol using General Procedure H), the title compound was prepared as a solid (mp=155-159° C.). The reaction was monitored by tlc (Rf=0.4 in EtOAc) and the product was purified by silica gel chromatography using EtOAc as the eluent.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US06211235B1
出典データセットuspto-grants-2001_04
ORD IDord-a0e03da8ca464209b970eef01cadd5be
出典メモuspto-grants-2001_04