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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 454329생성일: 2026년 10월 25일

Triethylamine → HCID 178496565, 화합물

https://huagongshe.com/reaction/454329

반응식

참여 물질

역할이름HCID투입량
반응물TriethylamineHCID 8471—
반응물Tri-o-tolylphosphineHCID 80271—
반응물5-Bromo-4-methylpyridine-2-carbonitrileHCID 53395468—
반응물HCID 178496566HCID 178496566—
반응물HCID 178496569HCID 178496569—
촉매Bis(dibenzylideneacetone)palladiumHCID 9811564—
용매DimethylformamideHCID 6228—
생성물HCID 178496565HCID 17849656594%

반응 조건

온도100 °C

반응 단계

5-(8-(((trans)-4-Methoxycyclohexyl)methyl)-7-oxo-5,6,7,8-tetrahydropyrazino[2,3-b]pyrazin-2-yl)-4-methylpicolinonitrile. 1-(((trans)-4-Methoxycyclohexyl)methyl)-7-(trimethylstannyl)-3,4-dihydropyrazino[2,3-b]pyrazin-2(1H)-one (0.721 g, 1.64 mmol), 5-bromo-4-methylpicolinonitrile (0.323 g, 1.64 mmol), tris(dibenzylideneacetone)dipalladium(0) (0.150 g, 0.164 mmol), triethylamine (0.687 mL, 4.93 mmol), tri-ortho-toylphosphine (0.100 g, 0.328 mmol) and dimethylformamide (8 mL) were combined in a sealed reaction vessel. Nitrogen was bubbled through the reaction for 5 min and reaction was heated at 100° C. for 3 h. Reaction is filtered, concentrated and purified by silica gel column chromatography (0-80% ethyl acetate in hexanes). Fractions were combined and concentrated to afford the crude title compound used directly for next step (0.607 g, 1.55 mmol, 94% yield). MS (ESI) m/z 393.5 [M+1]+.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08492381B2
출처 데이터셋uspto-grants-2013_07
ORD IDord-d1e37b2556ce4c64a3efd55cefa4fba0
출처 메모uspto-grants-2013_07