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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 719477생성일: 2026년 10월 26일

Trifluoroacetic acid → 1-{4-[1-(4-Methanesulfonyl-phenyl)-1H-pyrazolo[3,4-d]pyrimidin-4-yloxy]-piperidin-1-yl}-butan-2-one

https://huagongshe.com/reaction/719477

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참여 물질

역할이름HCID투입량
반응물Trifluoroacetic acidHCID 6422—
반응물TriethylamineHCID 8471—
반응물1-Bromo-2-butanoneHCID 13156—
반응물1-(4-Methanesulfonyl-phenyl)-4-(piperidin-4-yloxy)-1H-pyrazolo[3,4-d]pyrimidine hydrochlorideHCID 21897774—
용매WaterHCID 962—
용매AcetonitrileHCID 6342—
용매1,4-DioxaneHCID 31275—
생성물1-{4-[1-(4-Methanesulfonyl-phenyl)-1H-pyrazolo[3,4-d]pyrimidin-4-yloxy]-piperidin-1-yl}-butan-2-oneHCID 2189748919%

반응 조건

온도100 °C

반응 단계

To a solution of 1-(4-methanesulfonyl-phenyl)-4-(piperidin-4-yloxy)-1H-pyrazolo[3,4-d]pyrimidine hydrochloride (30.0 mg, 0.073 m mmol) and Et3N (35 μL) in dioxane (1.5 mL) was added bromomethyl ethyl ketone (22 μL, 0.219 mmol). The mixture was heated by microwave irradiation at 100° C. for 10 min. The mixture was diluted with CH3CN (3 mL) and purified by reverse-phase HPLC: Phenomenex® Luna C18 column (10μ, 250×21.2 mm), 5% (v/v) CH3CN (containing 1% v/v TFA) in H2O (containing 1% v/v TFA) gradient to 95% H2O, 20 mL/min, λ=214 nm to give Compound A168 (7.8 mg, 0.014 mmol, 19% yield) isolated as a white solid. HPLC/MS: Alltech® Prevail C18 column (5μ, 50×4.6 mm), 5% v/v CH3CN (containing 1% v/v TFA) in H2O (containing 1% v/v TFA) gradient to 99% v/v CH3CN in H2O, 3.5 mL/min, tr=1.69 min, ESI+=444.3 (M+H).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07132426B2
출처 데이터셋uspto-grants-2006_11
ORD IDord-04371e20a23f4e7b80a74606a1d3abcf
출처 메모uspto-grants-2006_11