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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 522986생성일: 2026년 10월 24일

Cesium carbonate → N-tert-butyl-2-(methyl(pyridin-3-yl)amino)-5-((2-(trimethylsilyl)ethoxy)methyl)-5H-pyrrolo[2,3-b]pyrazine-7-carboxamide

https://huagongshe.com/ko/reaction/522986

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참여 물질

역할이름HCID투입량
반응물Cesium carbonateHCID 10796—
반응물N-Methyl-3-pyridinamineHCID 140376—
반응물1,1'-(9,9-Dimethyl-9H-xanthene-4,5-diyl)bis(1,1-diphenylphosphine)HCID 636044—
반응물2-bromo-N-(tert-butyl)-5-((2-(trimethylsilyl)ethoxy)methyl)-5H-pyrrolo[2,3-b]pyrazine-7-carboxamideHCID 71575645—
촉매Bis(dibenzylideneacetone)palladiumHCID 9811564—
용매1,4-DioxaneHCID 31275—
생성물N-tert-butyl-2-(methyl(pyridin-3-yl)amino)-5-((2-(trimethylsilyl)ethoxy)methyl)-5H-pyrrolo[2,3-b]pyrazine-7-carboxamideHCID 9004121229%

반응 조건

온도150 °C

반응 단계

A mixture of 2-bromo-N-tert-butyl-5-((2-(trimethylsilyl)ethoxy)methyl)-5H-pyrrolo[2,3-b]pyrazine-7-carboxamide (125 mg, 292 μmol), N-methylpyridin-3-amine (47.4 mg, 439 μmol), xantphos (50.8 mg, 87.7 μmol), Pd2(dba)3 (26.8 mg, 29.2 μmol) and cesium carbonate (191 mg, 585 μmol) in dioxane (2 mL) was heated in a microwave at 150° C. for 20 min. The mixture was cooled and then filtered through a pad of celite. The filtrate was concentrated in vacuo then purified by chromatography (silica, ethyl acetate in hexanes) to give N-tert-butyl-2-(methyl(pyridin-3-yl)amino)-5-((2-(trimethylsilyl)ethoxy)methyl)-5H-pyrrolo[2,3-b]pyrazine-7-carboxamide (38 mg, 83.6 μmol, 29%) as a yellow gum. (EI/CI) m/z: 455.4 [M+H].

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US09334278B2
출처 데이터셋uspto-grants-2016_05
ORD IDord-79dc9df8e7b743ae89ee0b36e29d3630
출처 메모uspto-grants-2016_05