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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 600277생성일: 2026년 10월 25일

Triethylamine → 2-{3-[2-Fluoro-5-(4-oxo-3,4-dihydro-phthalazin-1-ylmethyl)-phenyl]-urido}-propionic acid

https://huagongshe.com/reaction/600277

반응식

참여 물질

역할이름HCID투입량
반응물TriethylamineHCID 8471—
반응물Ethyl AcetateHCID 8857—
반응물D-Aspartic AcidHCID 83887—
반응물4-(4-Fluoro-3-isocyanato-benzyl)-2H-phthalazin-1-oneHCID 59856545—
용매DichloromethaneHCID 6344—
생성물2-{3-[2-Fluoro-5-(4-oxo-3,4-dihydro-phthalazin-1-ylmethyl)-phenyl]-urido}-propionic acidHCID 68978764—

반응 단계

To a suspension of 4-(3-isocyanato-benzyl)-2H-phthalazin-1-one (2)(1.4 g, 4.7 mmol) in dry DCM (40 ml) was added D-aspartic acid (0.455 g, 5.0 mmol), followed by triethylamine (1.4 ml, 10.0 mmol). The reaction was stirred at room temperature for 4 days. The reaction mixture was then filtered. The filtrate was then diluted with water (20 ml) and washed twice with DCM (2×20 ml). The combined DCM layers were dried over sodium sulfate and then concentrated in vacuo to afford a crude oil which was subjected to flash chromatography eluent neat ethyl acetate to remove impurity and the then 1:1 ethyl acetate/methanol to remove the desired component. (Rf of 0.2 in 1:1 ethyl acetate methanol). Single peak in LC-MS analysis, (0.79 g) requiring no further purification; m/z (LC-MS, ESP), RT=2.70 (M+H) 384;

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07902193B2
출처 데이터셋uspto-grants-2011_03
ORD IDord-e4cb7af33a5c4bd5a56a5f4010e4c443
출처 메모uspto-grants-2011_03