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HRID 353623作成日:2026年10月26日

Sodium Carbonate → Methyl 6-[(2,2-diphenylethyl)amino]-9{-(2R,3R,4R,5S)-5-[(ethylamino)carbonyl]-3,4-dihydroxytetrahydro-2-furanyl}-9H-purine-2-carboxylate

https://huagongshe.com/reaction/353623

反応式

関与物質

役割名称HCID仕込み量
反応物Sodium CarbonateHCID 10340—
反応物methyl 9-{(2R,3R,4R,5S)-3,4-bis(benzoyloxy)-5-[(ethylamino)carbonyl]-tetrahydro-2-furanyl}-6-[(2,2-diphenylethyl)amino]-9H-purine-2-carboxylateHCID 18345898—
溶媒MethanolHCID 887—
生成物Methyl 6-[(2,2-diphenylethyl)amino]-9{-(2R,3R,4R,5S)-5-[(ethylamino)carbonyl]-3,4-dihydroxytetrahydro-2-furanyl}-9H-purine-2-carboxylateHCID 1834589798%

反応手順

A solution of methyl 9-{(2R,3R,4R,5S)-3,4-bis(benzoyloxy)-5-[(ethylamino)carbonyl]-tetrahydro-2-furanyl}-6-[(2,2-diphenylethyl)amino]-9H-purine-2-carboxylate (Preparation 8) (3.4 g, 4.5 mmol) and sodium carbonate (50 mg) in dry methanol (60 ml) was stirred at room temperature for four hours Solvent was removed under reduced pressure and the residue taken up in a mixture of dichloromethane:methanol (95:5, by volume, 60 ml). Inorganic salts were filtered off and the filtrate evaporated under reduced pressure. The residue was triturated with diethyl ether, filtered off and dried to yield the title compound as a white solid, (2.4 g, 98%).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US06753322B2
出典データセットuspto-grants-2004_06
ORD IDord-137a9acaae13499b80f02123386d5476
出典メモuspto-grants-2004_06