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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
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
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| 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-carboxylate | HCID 10187396 | — |
| 反応物 | HCID 178511674 | HCID 178511674 | — |
| 溶媒 | Dichloromethane | HCID 6344 | — |
| 生成物 | HCID 178465184 | HCID 178465184 | 79.5% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 特許番号 | US06753322B2 |
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| 出典データセット | uspto-grants-2004_06 |
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| ORD ID | ord-126fb2c937f44c4da48f0d0801988004 |
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| 出典メモ | uspto-grants-2004_06 |
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