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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 2361731생성일: 2026년 10월 27일

Acetonitrile → 9-[(2R)2-Deoxy-3,5-di-O-isobutyryl-2-C-ethynyl-2-fluoro-beta-D-erythro-pentofuranosyl]guanine

https://huagongshe.com/reaction/2361731

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참여 물질

역할이름HCID투입량
반응물AcetonitrileHCID 6342—
반응물Isobutyric anhydrideHCID 7346—
반응물TriethylamineHCID 8471—
반응물Sodium BicarbonateHCID 516892—
반응물9-[(2R)-2-Deoxy-2-C-ethynyl-2-fluoro-beta-D-erythro-furanosyl]-guanineHCID 136343928—
촉매4-(Dimethylamino)pyridineHCID 14284—
용매Ethyl AcetateHCID 8857—
생성물9-[(2R)2-Deoxy-3,5-di-O-isobutyryl-2-C-ethynyl-2-fluoro-beta-D-erythro-pentofuranosyl]guanineHCID 136195920—

반응 단계

A solution of 9-[(2R)-2-Deoxy-2-C-ethynyl-2-fluoro-β-D-erythro-furanosyl]guanine (0.16 mmol), 4-dimethylaminopyridine (0.01 mmol), triethylamine (0.48 mmol) and isobutyric anhydride (0.48 mmol), in acetonitrile (1 ml) was stirred at room temperature for 6 hours. The reaction mixture was hydrolysed with a NaHCO3 saturated solution. Ethyl acetate was added. The organic phase was separated, washed with NaCl saturated solution, dried over Na2SO4, filtered and concentrated under reduced pressure. The crude material was purified by flash column chromatography (DCM/EtOH) to yield the title compound White powder. Molecular Formula C20H24FN5O6 1H NMR (DMSO-d6, 400 MHz) δ (ppm) 1.02-1.22 (m, 12H), 2.53-2.59 (m, 1H), 2.65-2.70 (m, 1H), 4.04 (d, J=4.77 Hz, 1H), 4.35-4.40 (m, 3H), 5.88-5.94 (dd, J=9.39 Hz and J=8.21 Hz, 1H), 6.21-6.25 (d, J=17.28 Hz, 1H), 6.58 (s, 2H), 7.09 (s, 1H), 10.82 (s, 1H). Scan ES+ 450.0 (M+H)+, UV λmax 251 nm

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08691788B2
출처 데이터셋uspto-grants-2014_04
ORD IDord-801d79949f21439582fb4f32c3bc1388
출처 메모uspto-grants-2014_04