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HRID 353634作成日:2026年10月26日

Methyl 6-[(2,2-diphenylethyl)amino]-9-{(2R,3R,4S,5S)-5-[(ethylamino)carbonyl]-3,4-dihydroxytetrahydro-2-furanyl}-9H-purine-2-carboxylate → HCID 178465184、化合物

https://huagongshe.com/reaction/353634

反応式

関与物質

役割名称HCID仕込み量
反応物Methyl 6-[(2,2-diphenylethyl)amino]-9-{(2R,3R,4S,5S)-5-[(ethylamino)carbonyl]-3,4-dihydroxytetrahydro-2-furanyl}-9H-purine-2-carboxylateHCID 10187396—
反応物HCID 178511674HCID 178511674—
溶媒DichloromethaneHCID 6344—
生成物HCID 178465184HCID 17846518479.5%

反応条件

温度105 °C

反応手順

A mixture of methyl 6-[(2,2-diphenylethyl)amino]-9-{(2R,3R,4S,5S)-5-[(ethylamino)carbonyl]-3,4-dihydroxytetrahydro-2-furanyl}-9H-purine-2-carboxylate (Preparation 9) (0.35 g, 0.64 mmol) and trans-1,4-diaminocyclohexane (0.6 g, 6.14 mmol) was heated at 105° C. for 3 hours. The mixture was dissolved in a little dichloromethane and purified by column chromatography on silica gel eluting with a gradient system of dichloromethane:methanol:concentrated aqueous ammonia (80:20:1.2, by volume) changing to dichloromethane:methanol:concentrated aqueous ammonia (88:12:2, by volume). After evaporation of appropriate fractions the residue was triturated with diethyl ether, filtered and dried to yield the target compound as a white solid, (0.32 g, 79%).

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-126fb2c937f44c4da48f0d0801988004
出典メモuspto-grants-2004_06