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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 72705생성일: 2026년 10월 24일

Sodium Bicarbonate → 4-(3-fluoroazetidin-1-yl)-3-iodo-1-methyl-1H-pyrazolo[3,4-d]pyrimidine

https://huagongshe.com/ko/reaction/72705

반응식

참여 물질

역할이름HCID투입량
반응물Sodium BicarbonateHCID 516892—
반응물3-FluoroazetidineHCID 3603542—
반응물4-chloro-3-iodo-1-methyl-1H-pyrazolo[3,4-d]pyrimidineHCID 86712561—
용매TetrahydrofuranHCID 8028—
생성물4-(3-fluoroazetidin-1-yl)-3-iodo-1-methyl-1H-pyrazolo[3,4-d]pyrimidineHCID 71114419—

반응 단계

4-Chloro-3-iodo-1-methyl-1H-pyrazolo[3,4-d]pyrimidine (C9) (2.00 g, 6.79 mmol), 3-fluoroazetidine (833 mg, 7.46 mmol), saturated aqueous sodium bicarbonate solution (30 mL), and tetrahydrofuran (40 mL) were combined and allowed to stir at room temperature for 18 hours. After removal of volatiles in vacuo, the residue was diluted with water. Filtration provided the product as a tan solid. Yield: 1.91 g, 5.73 mmol, 84%. LCMS m/z 334.0 (M+1). 1H NMR (400 MHz, DMSO-d6) δ 3.91 (s, 3H), 4.47-4.63 (m, 2H), 4.75-4.90 (m, 2H), 5.44-5.64 (m, 1H, JHF=58.0 Hz), 8.31 (s, 1H).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08829010B2
출처 데이터셋uspto-grants-2014_09
ORD IDord-556b893a729546d8a1b1ce2dd4e70ef2
출처 메모uspto-grants-2014_09