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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 716058생성일: 2026년 10월 27일

(Methylsulfonyl)acetonitrile → 2-(methylsulfonyl)-3-(4-(7-pivaloyl-5-((2-(trimethylsilyl)ethoxy) methyl)-5H-pyrrolo[2,3-b]pyrazin-2-ylamino)phenyl)acrylonitrile

https://huagongshe.com/reaction/716058

반응식

참여 물질

역할이름HCID투입량
반응물(Methylsulfonyl)acetonitrileHCID 75283—
반응물Piperidine, acetateHCID 9793820—
반응물4-(7-pivaloyl-5-((2-(trimethylsilyl)ethoxy)methyl)-5H-pyrrolo[2,3-b]pyrazin-2-ylamino)benzaldehydeHCID 86712123—
용매EthanolHCID 702—
생성물2-(methylsulfonyl)-3-(4-(7-pivaloyl-5-((2-(trimethylsilyl)ethoxy) methyl)-5H-pyrrolo[2,3-b]pyrazin-2-ylamino)phenyl)acrylonitrileHCID 7101440564%

반응 단계

To a 10 ml seal tube, 4-(7-pivaloyl-5-((2-(trimethylsilyl)ethoxy)methyl)-5H-pyrrolo[2,3-b]pyrazin-2-ylamino)benzaldehyde (0.1 g, 0.00022 mol) and 2-(methylsulfonyl)acetonitrile (0.105 g, 0.00088 mol) were taken in ethanol (5 ml). Piperidine acetate (3.3 M solution in water) (1.0 ml) was added dropwise at RT. After completion of the addition, reaction mixture was refluxed for 24 hr. After completion of the reaction, ethanol was distilled out to obtain crude product. The crude product was purified by column chromatography using 30% ethyl acetate in hexanes to yield 0.078 g of 2-(methylsulfonyl)-3-(4-(7-pivaloyl-5-((2-(trimethylsilyl)ethoxy)methyl)-5H-pyrrolo[2,3-b]pyrazin-2-ylamino)phenyl)acrylonitrile which was converted to the title compound as described above.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US09187487B2
출처 데이터셋uspto-grants-2015_11
ORD IDord-8c08021df77140a7849b74eb81e1735e
출처 메모uspto-grants-2015_11