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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 11629생성일: 2026년 10월 24일

Triethylamine → 3-[3-(5-Chloro-2-{2-[4-(4-fluoro-benzyl)-(2R)-2-methyl-piperazin-1-yl]-2-oxo-ethoxy}-phenyl)-ureido]-propionic Acid Methyl Ester

https://huagongshe.com/ko/reaction/11629

반응식

참여 물질

역할이름HCID투입량
반응물TriethylamineHCID 8471—
반응물Methyl 3-aminopropanoate hydrochlorideHCID 2734767—
반응물(5-Chloro-2-(2-[4-(4-Fluoro-Benzyl)-(2R)-2-Methyl-Piperazin-1-Yl]-2-Oxo-Ethoxy}-Phenyl)-Carbamic Acid 4-Nitro-Phenyl EsterHCID 69655875—
용매MethanolHCID 887—
생성물3-[3-(5-Chloro-2-{2-[4-(4-fluoro-benzyl)-(2R)-2-methyl-piperazin-1-yl]-2-oxo-ethoxy}-phenyl)-ureido]-propionic Acid Methyl EsterHCID 6965537180%

반응 단계

To a solution of (5-chloro-2-{2-[4-(4-fluoro-benzyl)-(2R)-2-methyl-piperazin-1-yl]-2-oxo-ethoxy}-phenyl)-carbamic acid 4-nitro-phenyl ester (0.10 g, 0.18 mmol) in methanol was added β-alanine methyl ester hydrochloride (0.038 g, 0.27 mmol) and triethylamine (0.038 mL, 0.27 mmol). The reaction was stirred at ambient temperature overnight. The reaction was concentrated and purified via chromatography on silica gel to give the title compound (0.075 g).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07098212B2
출처 데이터셋uspto-grants-2006_08
ORD IDord-7f71fd0844e740eab34efa62eff663d6
출처 메모uspto-grants-2006_08