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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1055028생성일: 2026년 10월 25일

Triethylamine → 7-chloro-2-((1-(4-methoxybenzyl)-5-(pyrrolidin-1-yl)-1H-1,2,4-triazol-3-yl)ethynyl)quinoxaline

https://huagongshe.com/reaction/1055028

반응식

참여 물질

역할이름HCID투입량
반응물TriethylamineHCID 8471—
반응물2,7-DichloroquinoxalineHCID 2758223—
반응물3-ethynyl-1-(4-methoxy-benzyl)-5-pyrrolidin-1-yl-1H-[1,2,4]triazoleHCID 90025517—
촉매TriphenylphosphineHCID 11776—
촉매Copper(1+) iodide; Copper(I) iodide; Cuprous iodide; Cuprous iodide (CuI)HCID 24350—
촉매HCID 178418476HCID 178418476—
용매TetrahydrofuranHCID 8028—
생성물7-chloro-2-((1-(4-methoxybenzyl)-5-(pyrrolidin-1-yl)-1H-1,2,4-triazol-3-yl)ethynyl)quinoxalineHCID 9001743649.1%

반응 단계

A mixture of 3-ethynyl-1-(4-methoxybenzyl)-5-(pyrrolidin-1-yl)-1H-1,2,4-triazole (115 mg, 407 μmol, Eq: 1.00), 2,7-dichloroquinoxaline (89.2 mg, 448 μmol, Eq: 1.1) and triethylamine (61.8 mg, 85.2 μl, 611 μmol, Eq: 1.5) in tetrahydrofuran (3 ml) was purged with argon, then copper (I) iodide (3.1 mg, 16.3 μmol, Eq: 0.04), bis(triphenylphosphine)palladium(II) chloride (11.4 mg, 16.3 μmol, Eq: 0.04) and triphenylphosphine (4.27 mg, 16.3 μmol, Eq: 0.04) were added, the vessel was capped and heated for 18 hours to 75° C. The crude material was applied on silica gel and purified by flash chromatography to give 7-Chloro-2-[1-(4-methoxy-benzyl)-5-pyrrolidin-1-yl-1H-[1,2,4]triazol-3-ylethynyl]-quinoxaline (89 mg, 49.1%) as yellow solid. MS: m/z=445.4 (M+H+)

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US09394311B2
출처 데이터셋uspto-grants-2016_07
ORD IDord-082ba8a0c9924900b87effe9fef59afd
출처 메모uspto-grants-2016_07