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
참여 물질
| 역할 | 이름 | HCID | 투입량 |
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| 반응물 | (Methylsulfonyl)acetonitrile | HCID 75283 | — |
| 반응물 | Piperidine, acetate | HCID 9793820 | — |
| 반응물 | 4-(7-pivaloyl-5-((2-(trimethylsilyl)ethoxy)methyl)-5H-pyrrolo[2,3-b]pyrazin-2-ylamino)benzaldehyde | HCID 86712123 | — |
| 용매 | Ethanol | HCID 702 | — |
| 생성물 | 2-(methylsulfonyl)-3-(4-(7-pivaloyl-5-((2-(trimethylsilyl)ethoxy) methyl)-5H-pyrrolo[2,3-b]pyrazin-2-ylamino)phenyl)acrylonitrile | HCID 71014405 | 64% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US09187487B2 |
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| 출처 데이터셋 | uspto-grants-2015_11 |
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| ORD ID | ord-8c08021df77140a7849b74eb81e1735e |
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| 출처 메모 | uspto-grants-2015_11 |
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