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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1783201생성일: 2026년 10월 23일

Triethylamine → N1-{(1S,2R)-1-(3,5-difluorobenzyl)-3-[(2-furylmethyl)amino]-2-hydroxypropyl)-5-methyl-N3,N3-dipropylisophthalamide

https://huagongshe.com/ko/reaction/1783201

반응식

참여 물질

역할이름HCID투입량
반응물TriethylamineHCID 8471—
반응물3-FuraldehydeHCID 10351—
반응물N1-[(1S,2R)-3-amino-1-(3,5-difluorobenzyl)-2-hydroxypropyl]-5-methyl-N3,N3-dipropylisophthalamide Acetic Acid SaltHCID 68609581—
촉매PalladiumHCID 23938—
용매EthanolHCID 702—
생성물N1-{(1S,2R)-1-(3,5-difluorobenzyl)-3-[(2-furylmethyl)amino]-2-hydroxypropyl)-5-methyl-N3,N3-dipropylisophthalamideHCID 10280514—

반응 조건

온도22.5 °C

반응 단계

N1-[(1S,2R)-3-amino-1-(3,5-difluorobenzyl)-2-hydroxypropyl]-5-methyl-N3,N3-dipropylisophthalamide acetic acid salt (XVI, EXAMPLE 168, 76 mg, 0.146 mmol) is dissolved in absolute ethanol (2 mL). 3-Furaldehyde (20 microL, 0.231 mmol) and triethylamine (30 microL, 0.215 mmol) are added via syringe, with stirring at 20-25 degrees C. After 10 minutes, palladium on carbon 122 mg, 5 weight %) is added and the mixture placed under a hydrogen atmosphere (50 psi) and shaken for 20 minutes. The resulting mixture is then filtered through diatomaceous earth, with ethanol washings. The filtrate is purified by flash chromatography (2-10% methanol/methylene chloride) to give purified title compound, MS (MH+)=542.2.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07498436B2
출처 데이터셋uspto-grants-2009_03
ORD IDord-b81deedf452447e8891a1cb795db847b
출처 메모uspto-grants-2009_03