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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 434409생성일: 2026년 10월 24일

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

https://huagongshe.com/ko/reaction/434409

반응식

참여 물질

역할이름HCID투입량
반응물Hydrochloric AcidHCID 313—
반응물1,1'-CarbonyldiimidazoleHCID 68263—
반응물Tyrosine Methyl EsterHCID 70652—
반응물[Ethoxy(4-phenylbutyl)phosphoryl]acetic acidHCID 13136848—
용매MethanolHCID 887—
용매AcetonitrileHCID 6342—
용매TriethylamineHCID 8471—
생성물N-[[ethoxy(4-phenylbutyl)phosphinyl]acetyl]-L-tyrosine, methyl esterHCID 13171305088%

반응 조건

온도0 °C

반응 단계

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.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US04396772
출처 데이터셋uspto-grants-1983_08
ORD IDord-37fd470cc21344d8ba7464aa0b158bd6
출처 메모uspto-grants-1983_08