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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 58566생성일: 2026년 10월 24일

Diisopropylethylamine → N1-(2-(5-chloro-1H-indol-3-yl)ethyl)-N2-(2-hydroxy-1-phenylethyl)oxalamide

https://huagongshe.com/ko/reaction/58566

반응식

참여 물질

역할이름HCID투입량
반응물DiisopropylethylamineHCID 81531—
반응물5-Chloro-1H-indole-3-ethylamine monohydrochlorideHCID 2827494—
반응물Methanaminium, N-((dimethylamino)(3H-1,2,3-triazolo(4,5-b)pyridin-3-yloxy)methylene)-N-methyl-, hexafluorophosphate(1-) (1:1)HCID 9886157—
반응물2-(2-Hydroxy-1-phenylethylamino)-2-oxoacetic acidHCID 66831701—
용매DimethylformamideHCID 6228—
생성물N1-(2-(5-chloro-1H-indol-3-yl)ethyl)-N2-(2-hydroxy-1-phenylethyl)oxalamideHCID 66831872104.6%

반응 단계

The mixture of 2-(5-chloro-1H-indol-3-yl)ethanamine hydrochloride (0.256 g; 1.09 mmol), 2-(2-hydroxy-1-phenylethylamino)-2-oxoacetic acid (0.250 g; 1.19 mmol), HATU (0.413 g: 1.09 mmol) and N,N-diisopropylethylamine (0.474 mL; 2.71 mmol) in DMF (5 mL) was stirred at room temperature overnight and was concentrated under reduced pressure. The residue was dissolved in dichloromethane and the organic layer was washed with water and was concentrated under reduced pressure. The crude material was purified by flash chromatography on silica gel (eluent 1 to 10% methanol in dichloromethane) to yield 0.440 g of N1-(2-(5-chloro-1H-indol-3-yl)ethyl)-N2-(2-hydroxy-1-phenylethyl)oxalamide as a white solid.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US09434722B2
출처 데이터셋uspto-grants-2016_09
ORD IDord-19028feb7b7e41659ec4d9ccc2adb556
출처 메모uspto-grants-2016_09