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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 222152생성일: 2026년 10월 24일

Pyridine → (1S,2S,4R)-4-{4-[(1S)-2,3-Dihydro-1H-inden-1-ylamino]-7H-pyrrolo[2,3-d]-pyrimidin-7-yl}-2-(hydroxymethyl)cyclopentyl acetate

https://huagongshe.com/ko/reaction/222152

반응식

참여 물질

역할이름HCID투입량
반응물PyridineHCID 1049—
반응물Pyridine, hydrofluoride (1:1)HCID 64774—
반응물Sodium BicarbonateHCID 516892—
반응물(1S,2S,4R)-2-({[tert-Butyl(dimethyl)silyl]oxy}methyl)-4-{4-[(1S)-2,3-dihydro-1H-inden-1-ylamino]-7H-pyrrolo[2,3-d]pyrimidin-7-yl)cyclopentyl acetateHCID 66618132—
반응물HCID 178435178HCID 178435178—
용매TetrahydrofuranHCID 8028—
생성물(1S,2S,4R)-4-{4-[(1S)-2,3-Dihydro-1H-inden-1-ylamino]-7H-pyrrolo[2,3-d]-pyrimidin-7-yl}-2-(hydroxymethyl)cyclopentyl acetateHCID 6661846080.5%

반응 단계

(1S,2S,4R)-2-({[tert-Butyl(dimethyl)silyl]oxy}methyl)-4-{4-[(1S)-2,3-dihydro-1H-inden-1-ylamino]-7H-pyrrolo[2,3-d]pyrimidin-7-yl}cyclopentyl acetate (3.66 g, 7.03 mmol) was dissolved in THF (31.3 mL) and pyridine (31.3 mL, 387 mmol) in a polypropylene vial and the solution was cooled to 0° C. Pyridine hydrofluoride (8.61 mL, 95.6 mmol) was added dropwise and the mixture was stirred at rt for 1 hour. The resulting solution was added dropwise into a solution of saturated aqueous sodium bicarbonate (150 mL), extracted with EtOAc (3×50 mL), dried with MgSO4, filtered, and concentrated in vacuo. The residue was purified via silica gel chromatography eluting with a gradient of 0 to 10% MeOH in DCM to afford the title compound (2.30 g, 80%). LC/MS: Rt=1.64 min, ES+ 407 (AA standard).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08207177B2
출처 데이터셋uspto-grants-2012_06
ORD IDord-88540a7c5556462287951b80405af45e
출처 메모uspto-grants-2012_06