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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 58694생성일: 2026년 10월 25일

Diisopropylethylamine → N-(2-(6-fluoro-1H-indol-3-yl)ethyl)-5-(3-fluorobenzyl)isoxazole-3-carboxamide

https://huagongshe.com/reaction/58694

반응식

참여 물질

역할이름HCID투입량
반응물DiisopropylethylamineHCID 81531—
반응물2-(6-fluoro-1H-indol-3-yl)ethanamineHCID 854024—
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—
생성물N-(2-(6-fluoro-1H-indol-3-yl)ethyl)-5-(3-fluorobenzyl)isoxazole-3-carboxamideHCID 6683176041%

반응 단계

A mixture of the 5-(3-fluorobenzyl)isoxazole-3-carboxylic acid (0.057 g; 0.257 mmol), 2-(6-fluoro-1H-indol-3-yl)ethanamine (0.051 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 0.040 g (41%) 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-9298647cc310416583ecc891d6960b78
출처 메모uspto-grants-2016_09