Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1426524생성일: 2026년 10월 27일
Acetonitrile → 3-Methyl-3-[4-(7H-pyrrolo[2,3-d]pyrimidin-4-yl)-1H-pyrazol-1-yl]butanenitrile
https://huagongshe.com/reaction/1426524
참여 물질
| 역할 | 이름 | HCID | 투입량 |
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| 반응물 | Acetonitrile | HCID 6342 | — |
| 반응물 | 1,8-Diazabicyclo(5.4.0)undec-7-ene | HCID 81184 | — |
| 반응물 | 3-Methyl-2-butenenitrile | HCID 94301 | — |
| 반응물 | 4-(1H-Pyrazol-4-yl)-7-(2-(trimethylsilyl)ethoxy)methyl-7 H-pyrrolo(2,3-d)-pyrimidine | HCID 42631346 | — |
| 생성물 | 3-Methyl-3-[4-(7H-pyrrolo[2,3-d]pyrimidin-4-yl)-1H-pyrazol-1-yl]butanenitrile | HCID 17754811 | — |
반응 단계
To a solution of 4-(1H-pyrazol-4-yl)-7-[2-(trimethylsilyl)ethoxy]methyl-7H-pyrrolo[2,3-d]-pyrimidine (0.216 g, 0.684 mmol) in ACN (4 mL, 0.08 mol) was added crude senecionitrile (0.111 g, 1.37 mmol), followed by DBU (200 mL, 0.002 mol) and the resulting mixture was heated to 60° C. for 23 hours. The mixture was cooled to room temperature and the ACN was evaporated. The mixture was diluted with ethyl acetate and washed with dilute HCl and brine. The organic solution was dried over sodium sulfate, filtered and concentrated. Purification by silica gel chromatography (ethyl acetate/hexanes) afforded the desired product.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US08933086B2 |
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| 출처 데이터셋 | uspto-grants-2015_01 |
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| ORD ID | ord-25459889e37e45a3929162cdd8b2b1e3 |
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| 출처 메모 | uspto-grants-2015_01 |
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