戻る
化工社化工社 化学情報印刷レポート · 研究参考用
HRID 6269作成日:2026年10月25日

Triphenylphosphine → (S)-2-[bis-(t-butoxycarbonyl)amino]-9-[3-benzyloxy-2-(diethoxyphosphorylmethoxy)propoxy]-6-methoxypurine

https://huagongshe.com/reaction/6269

反応式

関与物質

役割名称HCID仕込み量
反応物TriphenylphosphineHCID 11776—
反応物ethyl N-ethoxycarbonyliminocarbamateHCID 220568—
反応物2-[Bis-(t-butoxycarbonyl)amino]-9-hydroxy-6-methoxypurineHCID 14523966—
反応物diethyl (R)-[2-benzyloxy-1-(hydroxymethyl)ethoxy]methylphosphonateHCID 53890153—
溶媒TetrahydrofuranHCID 8028—
生成物(S)-2-[bis-(t-butoxycarbonyl)amino]-9-[3-benzyloxy-2-(diethoxyphosphorylmethoxy)propoxy]-6-methoxypurineHCID 5369661888.6%

反応手順

To a stirred solution of diethyl (R)-[2-benzyloxy-1-(hydroxymethyl)ethoxy]methylphosphonate (1.0 g, 3 mmol), triphenylphosphine (1.18 g, 4.5 mmol) and 2-[bis-(t-butoxycarbonyl)amino]-9-hydroxy-6-methoxypurine (1.15 g, 3 mmol) in dry THF (20 ml), cooled in ice and under a mitrogen atmosphere, was added, dropwise, diethyl azodicarboxylate (0.71 ml, 4.5 mmol). The resulting solution was allowed to warm to ambient temperature and left stirring for 16 hours. The solvent was evaporated under reduced pressure and the residue obtained chromatographed on silica gel using hexane/ethyl acetate 2:1 as eluant. The eluant was changed as follows: hexane/ethyl acetate 1:1, hexane/ethyl acetate 1:2 and finally to ethyl acetate to give (S)-2-[bis-(t-butoxycarbonyl)amino]-9-[3-benzyloxy-2-(diethoxyphosphorylmethoxy)propoxy]-6-methoxypurine as a colourless oil (1.85 g, 88%).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05247085
出典データセットuspto-grants-1993_09
ORD IDord-5bc3817b8fb84fdcb2e908b50be90647
出典メモuspto-grants-1993_09