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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 58696생성일: 2026년 10월 24일

2-(2-Aminoethyl)-5-methoxyindole → 5-(3-fluorobenzyl)-N-(2-(6-methoxy-1H-indol-3-yl)ethyl)isoxazole-3-carboxamide

https://huagongshe.com/ko/reaction/58696

반응식

참여 물질

역할이름HCID투입량
반응물2-(2-Aminoethyl)-5-methoxyindoleHCID 17654—
반응물DiisopropylethylamineHCID 81531—
반응물Methanaminium, N-((dimethylamino)(3H-1,2,3-triazolo(4,5-b)pyridin-3-yloxy)methylene)-N-methyl-, hexafluorophosphate(1-) (1:1)HCID 9886157—
반응물5-(3-Fluorobenzyl)isoxazole-3-carboxylic acidHCID 66832107—
용매DimethylformamideHCID 6228—
생성물5-(3-fluorobenzyl)-N-(2-(6-methoxy-1H-indol-3-yl)ethyl)isoxazole-3-carboxamideHCID 6683209038%

반응 단계

A solution of the 5-(3-fluorobenzyl)isoxazole-3-carboxylic acid (0.057 g; 0.257 mmol), 2-(6-methoxy-1H-indol-3-yl)ethanamine (0.054 g; 0.284 mmol), HATU (0.108 g; 0.284 mmol) and N,N-diisopropylethylamine (0.112 mL; 0.649 mmol) in DMF (3 mL), was stirred at room temperature overnight. The reaction mixture was partitioned between ethyl acetate and sodium hydrogen sulfate, the organic layer was washed with sodium carbonate, brine, dried and concentrated under reduced pressure. The crude mixture was purified by flash chromatography on silica (eluent 20 to 100% ethyl acetate in heptane) to yield 0.035 g (38%) of the title compound as a white solid.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US09434722B2
출처 데이터셋uspto-grants-2016_09
ORD IDord-de9f2b2e214b4f748ffb4c945caae68a
출처 메모uspto-grants-2016_09