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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

반응식

참여 물질

역할이름HCID투입량
반응물AcetonitrileHCID 6342—
반응물1,8-Diazabicyclo(5.4.0)undec-7-eneHCID 81184—
반응물3-Methyl-2-butenenitrileHCID 94301—
반응물4-(1H-Pyrazol-4-yl)-7-(2-(trimethylsilyl)ethoxy)methyl-7 H-pyrrolo(2,3-d)-pyrimidineHCID 42631346—
생성물3-Methyl-3-[4-(7H-pyrrolo[2,3-d]pyrimidin-4-yl)-1H-pyrazol-1-yl]butanenitrileHCID 17754811—

반응 조건

온도60 °C

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

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08933086B2
출처 데이터셋uspto-grants-2015_01
ORD IDord-25459889e37e45a3929162cdd8b2b1e3
출처 메모uspto-grants-2015_01