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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 552725생성일: 2026년 10월 27일

[(3aR,4R,6R,6aS)-6-(6-chloro-9H-purin-9-yl)-2,2-dimethyltetrahydro-3aH-cyclopenta[d][1,3]dioxol-4-yl]methyl acetate → [(3aR,4R,6R,6aS)-6-(6-isobutyl-9H-purin-9-yl)-2,2-dimethyltetrahydro-3aH-cyclopenta[d][1,3]dioxol-4-yl]methyl acetate

https://huagongshe.com/reaction/552725

반응식

참여 물질

역할이름HCID투입량
반응물[(3aR,4R,6R,6aS)-6-(6-chloro-9H-purin-9-yl)-2,2-dimethyltetrahydro-3aH-cyclopenta[d][1,3]dioxol-4-yl]methyl acetateHCID 86607316—
반응물HCID 178448254HCID 178448254—
촉매HCID 178418397HCID 178418397—
용매TetrahydrofuranHCID 8028—
생성물[(3aR,4R,6R,6aS)-6-(6-isobutyl-9H-purin-9-yl)-2,2-dimethyltetrahydro-3aH-cyclopenta[d][1,3]dioxol-4-yl]methyl acetateHCID 6716566945%

반응 조건

온도60 °C

반응 단계

To a solution of [(3aR,4R,6R,6aS)-6-(6-chloro-9H-purin-9-yl)-2,2-dimethyltetrahydro-3aH-cyclopenta[d][1,3]dioxol-4-yl]methyl acetate (250.0 mg, 0.68 mmol) in degassed THF (6 mL) under nitrogen was added Pd(PPh3)4 (44 mg, 0.038 mmol) followed by 0.5 M of isobutylzinc bromide in tetrahydrofuran (2.04 mL) dropwise over 15 min. The reaction was heated at 60° C. for 1 hour. The reaction was cooled then quenched with saturated aq NH4Cl, extracted with EtOAc and the organic phase was washed with saturated aq EDTA.Na2 solution then water. The organic phase was concentrated and the residue purified by flash chromatography (0 to 100% EtOAc/DCM) to provide the title compound (120 mg, 45%).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07951810B2
출처 데이터셋uspto-grants-2011_05
ORD IDord-e2a4ea5ed84744fba7c1d2065205bbe5
출처 메모uspto-grants-2011_05