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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 339291생성일: 2026년 10월 24일

1-Ethyl-3-(3'-dimethylaminopropyl)carbodiimide → (S)-methyl 2-((4Z,7Z,10Z,13Z,16Z,19Z)-docosa-4,7,10,13,16,19-hexaenamido)propanoate

https://huagongshe.com/ko/reaction/339291

반응식

참여 물질

역할이름HCID투입량
반응물1-Ethyl-3-(3'-dimethylaminopropyl)carbodiimideHCID 15908—
반응물DiisopropylethylamineHCID 81531—
반응물DoconexentHCID 445580—
반응물Alanine methyl ester hydrochlorideHCID 2733257—
용매AcetonitrileHCID 6342—
용매Ethyl AcetateHCID 8857—
생성물(S)-methyl 2-((4Z,7Z,10Z,13Z,16Z,19Z)-docosa-4,7,10,13,16,19-hexaenamido)propanoateHCID 980186079.3%

반응 단계

L-Alanine methyl ester hydrochloride (0.85 g, 6.1 mmol) was taken up in CH3CN (20 mL) along with (4Z,7Z,10Z,13Z,16Z,19Z)-docosa-4,7,10,13,16,19-hexaenoic acid (2.0 g, 6.1 mmol), EDCI (1.3 g, 6.72 mmol) and DIEA (1.3 mL). The resulting reaction mixture was stirred at room temperature for 2 h. It was then diluted with EtOAc and washed with dilute aqueous NaHCO3 and brine. The organic layer was dried over Na2SO4, filtered and concentrated under reduced pressure to afford (S)-methyl 2-((4Z,7Z,10Z,13Z,16Z,19Z)-docosa-4,7,10,13,16,19-hexaenamido)propanoate (2.0 g, 79%).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호USRE045261E1
출처 데이터셋uspto-grants-2014_11
ORD IDord-71a961c9ac104dbdb10e3c5b4f51c3c3
출처 메모uspto-grants-2014_11