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HRID 1031070作成日:2026年10月27日

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

https://huagongshe.com/reaction/1031070

反応式

関与物質

役割名称HCID仕込み量
反応物TriphenylphosphineHCID 11776—
反応物Diethyl azodicarboxylateHCID 5462977—
反応物Diethyl 2-hydroxyethylthiomethylphosphonateHCID 10376467—
反応物9-Hydroxy-6-phthalimidopurineHCID 14523970—
溶媒TetrahydrofuranHCID 8028—
生成物9-[2-(Diethoxyphosphorylmethylthio)ethoxy]-6-phthalimidopurineHCID 1981955856%

反応手順

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%).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05108994
出典データセットuspto-grants-1992_04
ORD IDord-404cbf1e8bf24a3e8bc3b8b66d880dab
出典メモuspto-grants-1992_04