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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1031070생성일: 2026년 10월 26일

Triphenylphosphine → 9-[2-(Diethoxyphosphorylmethylthio)ethoxy]-6-phthalimidopurine

https://huagongshe.com/reaction/1031070

반응식

참여 물질

역할이름HCID투입량
반응물TriphenylphosphineHCID 11776—
반응물Diethyl azodicarboxylateHCID 5462977—
반응물Diethyl 2-hydroxyethylthiomethylphosphonateHCID 10376467—
반응물9-Hydroxy-6-phthalimidopurineHCID 14523970—
용매TetrahydrofuranHCID 8028—
생성물9-[2-(Diethoxyphosphorylmethylthio)ethoxy]-6-phthalimidopurineHCID 1981955856%

반응 단계

A mixture of 9-hydroxy-6-phthalimidopurine (0.5 g, 2.2 mmol). diethyl-2-hydroxyethylthiomethylphosphonate (0.45 g. 2 mmol) and triphenylphosphine (0.52 g, 2 mmol) was dissolved in dry tetrahydrofuran (20 ml) and cooled to 0°-5° C. A solution of diethylazodicarboxylate (0.348 g, 2.0 mmol) in dry tetrahydrofuran (10 ml) was added dropwise with stirring, and after the addition was completed the reaction was stirred at room temperature for 18 hours. The solvent was then removed in vacuo, and the residue was purified by column chromatography on silica using ethyl acetate: methanol (98:2) as eluent to give 9-[2-(diethoxyphosphorylmethylthio)ethoxy]-6-phthalimidopurine (0.45 g 56%) as a white solid after crystallisation from acetone/diethyl ether, m.p. 115°-116° C.; γmax (EtOH) 271mm (s 14020) υmax (KBr) 3100, 3060, 2960, 2900, 1780, 1725, 1650, 1600, 1580, 1453, 1400, 1380, 1360, 1320, 1280, 1240, and 1200 cm-1 ; δH [(CD3)2SO] 1.25 (6H, t, J 7Hz 2 × CH3), 3.0 (2H, d, J 13Hz, PCH2S), 3.1 (2H, t, J 7Hz CH20, 4.0 (4H, m, 2 × CH2), 4.7 (2H, t, J 7Hz, CH2S), 8.1 (4H, m, Ar H), 9.0 (1H, s, 2H), 9.1 (1H, s, 8-H). (Found C, 48.65; H, 4.55; N, 14.23%. C20H22N5O6PS requires C,48.87; H, 4.51; N, 14.25%).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05108994
출처 데이터셋uspto-grants-1992_04
ORD IDord-404cbf1e8bf24a3e8bc3b8b66d880dab
출처 메모uspto-grants-1992_04