戻る
化工社化工社 化学情報印刷レポート · 研究参考用
HRID 434409作成日:2026年10月25日

Hydrochloric Acid → N-[[ethoxy(4-phenylbutyl)phosphinyl]acetyl]-L-tyrosine, methyl ester

https://huagongshe.com/reaction/434409

反応式

関与物質

役割名称HCID仕込み量
反応物Hydrochloric AcidHCID 313—
反応物1,1'-CarbonyldiimidazoleHCID 68263—
反応物Tyrosine Methyl EsterHCID 70652—
反応物[Ethoxy(4-phenylbutyl)phosphoryl]acetic acidHCID 13136848—
溶媒MethanolHCID 887—
溶媒AcetonitrileHCID 6342—
溶媒TriethylamineHCID 8471—
生成物N-[[ethoxy(4-phenylbutyl)phosphinyl]acetyl]-L-tyrosine, methyl esterHCID 13171305088%

反応条件

温度0 °C

反応手順

1,1'-Carbonyldiimidazole (0.56 g) was added portionwise to a cooled (0° C.) solution of [ethoxy(4-phenylbutyl)phosphinyl]acetic acid (0.98 g) in 70 ml of acetonitrile. This reaction mixture was stirred under argon at 0° C. for 1.5 hours. The HCl salt of L-tyrosine methyl ester (0.8 g) was dissolved in methanol and neutralized with triethylamine (0.35 g). This solution was concentrated in vacuo, dissolved in 10 ml of warm acetonitrile and added dropwise to the above solution of activated phosphinic acid ester sidechain. The reaction was stirred overnight under argon and then concentrated in vacuo. A solution of the pot residue in dichloromethane was washed (H2O, aqueous NaHCO3, brine), dried (MgSO4) and filtered to yield 1.4 g of N-[[ethoxy(4-phenylbutyl)phosphinyl]acetyl]-L-tyrosine, methyl ester.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US04396772
出典データセットuspto-grants-1983_08
ORD IDord-37fd470cc21344d8ba7464aa0b158bd6
出典メモuspto-grants-1983_08