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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1958433생성일: 2026년 10월 26일

Sodium hydride → 3-[1-(2-Fluoro-4-methanesulfonyl-phenyl)-1H-pyrazolo[3,4-d]pyrimidin-4-yloxy]-pyrrolidine-1-carboxylic acid tert-butyl ester

https://huagongshe.com/reaction/1958433

반응식

참여 물질

역할이름HCID투입량
반응물Sodium hydrideHCID 24758—
반응물1-Boc-3-pyrrolidinolHCID 4416939—
반응물4-Chloro-1-(2-fluoro-4-methanesulfonyl-phenyl)-1H-pyrazolo[3,4-d]pyrimidineHCID 21897661—
용매TetrahydrofuranHCID 8028—
생성물3-[1-(2-Fluoro-4-methanesulfonyl-phenyl)-1H-pyrazolo[3,4-d]pyrimidin-4-yloxy]-pyrrolidine-1-carboxylic acid tert-butyl esterHCID 5363041667.8%

반응 단계

A mixture of 3-hydroxy-pyrrolidine-1-carboxylic acid tert-butyl ester (431 mg, 2.3 mmol) and sodium hydride (92 mg, 3.82 mmol) in THF (10 mL) was stirred for 30 minutes at room temperature. Then 4-chloro-1-(2-fluoro-4-methanesulfonyl-phenyl)-1H-pyrazolo[3,4-d]pyrimidine (500 mg, 1.53 mmol) was added and stirred overnight at room temperature. The reaction mixture was quenched with water and the product extracted with ethyl acetate. The ethylacetate layer was dried over MgSO4, concentrated in vacuo, and purified by flash chromatography to afford compound A140 as a white solid (495 mg, 45%). Exact mass calculated for C21H24FN5O5S 477.15, found 478.2 (MH+).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08410119B2
출처 데이터셋uspto-grants-2013_04
ORD IDord-7d469ada9f3144df87831c0277e8cc34
출처 메모uspto-grants-2013_04