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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1426625생성일: 2026년 10월 27일

Acetonitrile → methyl 3-phenyl-3-[4-(7-[2-(trimethylsilyl)ethoxy]methyl-7H-pyrrolo[2,3-d]pyrimidin-4-yl)-1H-pyrazol-1-yl]-propanoate

https://huagongshe.com/reaction/1426625

반응식

참여 물질

역할이름HCID투입량
반응물AcetonitrileHCID 6342—
반응물1,8-Diazabicyclo(5.4.0)undec-7-eneHCID 81184—
반응물Methyl CinnamateHCID 637520—
반응물4-(1H-Pyrazol-4-yl)-7-(2-(trimethylsilyl)ethoxy)methyl-7 H-pyrrolo(2,3-d)-pyrimidineHCID 42631346—
생성물methyl 3-phenyl-3-[4-(7-[2-(trimethylsilyl)ethoxy]methyl-7H-pyrrolo[2,3-d]pyrimidin-4-yl)-1H-pyrazol-1-yl]-propanoateHCID 5747799770%

반응 단계

A solution of methyl (2E)-3-phenylacrylate (500 mg, 0.003 mol) in ACN (2 mL, 0.04 mol) was slowly added to a solution of 4-(1H-pyrazol-4-yl)-7-[2-(trimethylsilyl)ethoxy]methyl-7H-pyrrolo[2,3-d]pyrimidine (0.5 g, 0.002 mol) in ACN (2 mL, 0.04 mol) and DBU (500 mL, 0.003 mol). The reaction was stirred at room temperature over the weekend. The reaction was partitioned between water and EtOAc. The organic layer was washed with saturated sodium chloride, dried over MgSO4, filtered and concentrated to give an oil. The product was purified by FCC on silica gel using EtOAc/Hexane (1:2 to 1:1) gave methyl 3-phenyl-3-[4-(7-[2-(trimethylsilyl)ethoxy]methyl-7H-pyrrolo[2,3-d]pyrimidin-4-yl)-1H-pyrazol-1-yl]propanoate (500 mg, 70%) as a semisolid residue.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08933086B2
출처 데이터셋uspto-grants-2015_01
ORD IDord-ee73c5b6bacc4554896c53eaecfedba6
출처 메모uspto-grants-2015_01