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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 454343생성일: 2026년 10월 25일

2-(Oxan-4-yl)ethan-1-amine → 7-(1H-Pyrrolo[2,3-b]pyridin-5-yl)-1-(2-(tetrahydro-2h-pyran-4-yl)ethyl)-3,4-dihydropyrazino[2,3-b]pyrazin-2(1H)-one

https://huagongshe.com/reaction/454343

반응식

참여 물질

역할이름HCID투입량
반응물2-(Oxan-4-yl)ethan-1-amineHCID 2773198—
반응물Ethyl 2-(3,5-dibromopyrazin-2-ylamino)acetateHCID 57550751—
반응물Ethyl 2-(5-bromo-3-(2-(tetrahydro-2H-pyran-4-yl)ethylamino)pyrazin-2-ylamino)acetateHCID 86644650—
용매Dimethyl SulfoxideHCID 679—
생성물7-(1H-Pyrrolo[2,3-b]pyridin-5-yl)-1-(2-(tetrahydro-2h-pyran-4-yl)ethyl)-3,4-dihydropyrazino[2,3-b]pyrazin-2(1H)-oneHCID 5945306744%

반응 조건

온도150 °C

반응 단계

Ethyl 2-(5-bromo-3-(2-(tetrahydro-2H-pyran-4-yl)ethylamino)pyrazin-2-ylamino)acetate. Ethyl 2-(3,5-dibromopyrazin-2-ylamino)acetate (See Example 6.B) (1.0 g, 2.95 mmol) and 2-(tetrahydro-2H-pyran-4-yl)ethanamine (0.381 g, 2.95 mmol) were placed in a microwave via, dimethylsulfoxide (2 mL) was added and the resulting mixture was heated in a Biotage Emrys Optimizer microwave reactor at 150° C. for 3600 s. The crude reaction mixture was purified using silica gel chromatography (33% ethyl acetate in hexanes) to yield the title compound (0.5 g, 1.3 mmol, 44% yield). MS (ESI) m/z 387.1 [M]+, 389.1 [M+2]+.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08492381B2
출처 데이터셋uspto-grants-2013_07
ORD IDord-e5db7d76d0194828bf1df2eef50dbd00
출처 메모uspto-grants-2013_07