戻る
化工社化工社 化学情報印刷レポート · 研究参考用
HRID 25694作成日:2026年10月24日

Benzyloxycarbonyl-L-phenylalanine → benzyl (1S)-1-benzyl-2-[(3,3-diethoxypropyl)amino]-2-oxoethylcarbamate

https://huagongshe.com/ja/reaction/25694

反応式

関与物質

役割名称HCID仕込み量
反応物Benzyloxycarbonyl-L-phenylalanineHCID 70878—
反応物DiisopropylethylamineHCID 81531—
反応物1-Amino-3,3-diethoxypropaneHCID 521029—
反応物1,3-Propanediamine, N'-(ethylcarbonimidoyl)-N,N-dimethyl-, monohydrochlorideHCID 2723939—
反応物HCID 178418300HCID 178418300—
溶媒TetrahydrofuranHCID 8028—
生成物benzyl (1S)-1-benzyl-2-[(3,3-diethoxypropyl)amino]-2-oxoethylcarbamateHCID 5906590892%

反応手順

By using an analogous procedure to that described for Reference Example 13, N-(carbobenzyloxy)-L-phenylalanine (2 g, 6.68 mmol), hydroxybenzotriazole (903 mg, 6.68 mmol), 1-(3-dimethylaminopropyl)-3-ethylcarbodiimide hydrochloride 1.28 g, 6.68 mmol), 1-amino-3,3-diethoxypropane (935 mg, 6.36 mmol) and N,N-diisopropylethylamine (1.16 mL, 6.68 mmol) were reacted in anhydrous tetrahydrofuran (32 mL) at room temperature for 16 h, to provide benzyl (1S)-1-benzyl-2-[(3,3-diethoxypropyl)amino]-2-oxoethylcarbamate (2.5 g, 92%) as a white solid.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US06858591B2
出典データセットuspto-grants-2005_02
ORD IDord-d7e3ef9837ef482d892d5daff01e256a
出典メモuspto-grants-2005_02