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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1519690생성일: 2026년 10월 25일

Diisopropylethylamine → 1-(2,3-Dihydroxypropoxy)-4-[(4-{[1-methoxy-3-(methylamino)-1,3-dioxopropan-2-yl](methyl)carbamoyl}phenyl)ethynyl]benzene

https://huagongshe.com/reaction/1519690

반응식

참여 물질

역할이름HCID투입량
반응물DiisopropylethylamineHCID 81531—
반응물Sodium BicarbonateHCID 516892—
반응물Methanaminium, N-((dimethylamino)(3H-1,2,3-triazolo(4,5-b)pyridin-3-yloxy)methylene)-N-methyl-, hexafluorophosphate(1-) (1:1)HCID 9886157—
반응물4-{[4-(2,3-Dihydroxypropoxy)phenyl]ethynyl}benzoic acidHCID 71268145—
반응물N,N2,O-trimethyl-3-oxoserinamide hydrochlorideHCID 86679246—
용매DimethylformamideHCID 6228—
생성물1-(2,3-Dihydroxypropoxy)-4-[(4-{[1-methoxy-3-(methylamino)-1,3-dioxopropan-2-yl](methyl)carbamoyl}phenyl)ethynyl]benzeneHCID 712681478%

반응 조건

온도80 °C

반응 단계

N,N2,O-trimethyl-3-oxoserinamide hydrochloride (Intermediate 5-2, 0.13 g), HATU (0.17 g) and DIPEA (0.33 mL) were added to a DMF (2.0 mL) solution of 4-{[4-(2,3-dihydroxypropoxy)phenyl]ethynyl}benzoic acid (0.20 g) as obtained in Example 11-(2), and the mixture was stirred for 1 hour at 80° C. A saturated aqueous solution of sodium hydrogen carbonate was added to the reaction mixture, and the mixture was extracted with chloroform. The organic layer was washed with brine, and dried over anhydrous magnesium sulfate. The desiccant was filtered out, and the solvent was distilled off under reduced pressure. The resulting residue was purified by NH type silica gel column chromatography (gradient elution with ethyl acetate/methanol=99/1→88/12) to obtain 1-(2,3-dihydroxypropoxy)-4-[(4-{[1-methoxy-3-(methylamino)-1,3-dioxopropan-2-yl](methyl)carbamoyl}phenyl)ethynyl]benzene (white solid) (23 mg, 8.0%).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US09073821B2
출처 데이터셋uspto-grants-2015_07
ORD IDord-ef11bf582d124167b227aa3e6c5e1432
출처 메모uspto-grants-2015_07