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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 527921생성일: 2026년 10월 25일

Water → (R)-N-methyl-N-(4-(methylsulfonyl)phenyl)-1-(7-((2-(trimethylsilyl)ethoxy)methyl)-7H-pyrrolo[2,3-d]pyrimidin-4-yl)pyrrolidin-3-amine

https://huagongshe.com/reaction/527921

반응식

참여 물질

역할이름HCID투입량
반응물WaterHCID 962—
반응물Potassium CarbonateHCID 11430—
반응물1-Fluoro-4-(methylsulphonyl)benzeneHCID 67994—
반응물(R)-N-methyl-1-(7-((2-(trimethylsilyl)ethoxy)methyl)-7H-pyrrolo[2,3-d]pyrimidin-4-yl)pyrrolidin-3-amineHCID 66765875—
용매DimethylformamideHCID 6228—
생성물(R)-N-methyl-N-(4-(methylsulfonyl)phenyl)-1-(7-((2-(trimethylsilyl)ethoxy)methyl)-7H-pyrrolo[2,3-d]pyrimidin-4-yl)pyrrolidin-3-amineHCID 68027352—

반응 조건

온도120 °C

반응 단계

A mixture of (R)—N-methyl-1-(7-((2-(trimethylsilyl)ethoxy)methyl)-7H-pyrrolo[2,3-d]pyrimidin-4-yl)pyrrolidin-3-amine (100 mg, 0.287 mmol) and 1-fluoro-4-(methylsulfonyl)benzene (150 mg, 0.861 mmol) and K2CO3 (158 mg, 1.142 mmol) in DMF (2 mL) was stirred at 120° C. overnight and then cooled to ambient temperature, poured into water, and extracted with EtOAc. The EtOAc layer was concentrated, purified by preparative TLC to give the title compound.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US09346810B2
출처 데이터셋uspto-grants-2016_05
ORD IDord-8a6e48e266ee4ea581f1d4ab95eb4a3c
출처 메모uspto-grants-2016_05