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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 74866생성일: 2026년 10월 26일

Diisopropylethylamine → 2-[5-chloro-1-(p-tolylsulfonyl)pyrrolo[2,3-b]pyridin-3-yl]-5-fluoro-N-[(3S)-1-(2,2,2-trifluoroethyl)-3-piperidyl]pyrimidin-4-amine

https://huagongshe.com/reaction/74866

반응식

참여 물질

역할이름HCID투입량
반응물DiisopropylethylamineHCID 81531—
반응물2,2,2-Trifluoroethyl trichloromethanesulphonateHCID 90027—
반응물2-[5-chloro-1-(p-tolylsulfonyl)pyrrolo[2,3-b]pyridin-3-yl]-5-fluoro-N-[(3S)-3-piperidyl]pyrimidin-4-amineHCID 67285119—
용매DimethylformamideHCID 6228—
용매Sodium chloride; waterHCID 57417360—
생성물2-[5-chloro-1-(p-tolylsulfonyl)pyrrolo[2,3-b]pyridin-3-yl]-5-fluoro-N-[(3S)-1-(2,2,2-trifluoroethyl)-3-piperidyl]pyrimidin-4-amineHCID 67285830—

반응 단계

To a solution of 2-[5-chloro-1-(p-tolylsulfonyl)pyrrolo[5,4-b]pyridin-3-yl]-5-fluoro-N-[(3S)-3-piperidyl]pyrimidin-4-amine, 1c, (0.17 g, 0.34 mmol) in DMF (1.5 mL) was added 2,2,2-trifluoroethyl trichloromethanesulfonate (0.19 g, 0.68 mmol), followed by iPr2NEt (0.24 mL, 1.36 mmol). The reaction mixture was stirred at room temperature for 18 h. The mixture was poured into brine and extracted twice with EtOAc. The combined organic phases were washed twice with brine, dried (MgSO4), filtered, and concentrated in vacuo. The crude residue was purified by silica gel chromatography (0-10% MeOH/CH2Cl2) afforded the desired product, 3a, as a white solid.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08829007B2
출처 데이터셋uspto-grants-2014_09
ORD IDord-e5aa7fe842434d559e48fc806da251ee
출처 메모uspto-grants-2014_09