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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1009740생성일: 2026년 10월 25일

Diisopropylethylamine → N-(3-isoxazolyl)-2-[4-(6,7-dimethoxyquinolin-4-yloxy)phenyl]acetamide

https://huagongshe.com/reaction/1009740

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참여 물질

역할이름HCID투입량
반응물DiisopropylethylamineHCID 81531—
반응물3-IsoxazolamineHCID 1810216—
반응물1,3-Propanediamine, N'-(ethylcarbonimidoyl)-N,N-dimethyl-, monohydrochlorideHCID 2723939—
반응물2-(4-(6,7-Dimethoxyquinolin-4-yloxy)phenyl)acetic acidHCID 59647540—
반응물HCID 178526252HCID 178526252—
용매DimethylformamideHCID 6228—
생성물N-(3-isoxazolyl)-2-[4-(6,7-dimethoxyquinolin-4-yloxy)phenyl]acetamideHCID 6730453314.6%

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온도60 °C

반응 단계

1-(3-Dimethylaminopropyl)-3-ethylcarbodiimide hydrochloride (0.226 g) and 2-hydroxypyridine N-oxide (0.131 g) were added in turn to a stirred mixture of 2-[4-(6,7-dimethoxyquinolin-4-yloxy)phenyl]acetic acid (0.2 g), 3-aminoisoxazole (0.064 g), diisopropylethylamine (0.226 g) and DMF (3 ml) at ambient temperature. The resultant mixture was stirred and heated to 60° C. for 16 hours. The mixture was evaporated and the residue was purified by preparative HPLC using a Waters ‘Xterra’ reversed-phase column (5 microns silica, 30 mm diameter, 150 mm length) using decreasingly polar mixtures of water (containing 0.2% ammonium carbonate) and acetoliitrile as eluent. There was thus obtained the title compound (0.035 g); 1H NMR: (DMSOd6) 3.76 (s, 2H), 3.92 (s, 3H), 3.95 (s, 3H), 6.47 (d, 1H), 6.93 (d, 1H), 7.23 (d, 2H), 7.4 (s, 1H), 7.46 (d, 2H), 7.49 (s, 1H), 8.49 (d, 1H), 8.80 (d, 1H), 11.33 (br s, 1H); Mass Spectrum: M+H+ 406.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07973164B2
출처 데이터셋uspto-grants-2011_07
ORD IDord-8f22dcf49de44c3b9102b72f31afc206
출처 메모uspto-grants-2011_07