関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|
| 反応物 | Potassium Carbonate | HCID 11430 | — |
| 反応物 | 6-Chlorohexan-2-one | HCID 82468 | — |
| 反応物 | 7-allyl-3-methyl-3,7-dihydro-1H-purine-2,6-dione | HCID 973905 | — |
| 反応物 | Sodium borohydride | HCID 4311764 | — |
| 溶媒 | Ethanol | HCID 702 | — |
| 溶媒 | Dimethylformamide | HCID 6228 | — |
| 生成物 | 7-Allyl-1-(5-hydroxyhexyl)-3-methylxanthine | HCID 15023887 | — |
反応手順
To 11.8 g of 7-allyl-3-methyl-1-(5-oxyhexyl)-xanthine (prepared by alkylation of 7-allyl-3-methylxanthine with 1-chlorohexan-5-one in dimethylformamide in the presence of potassium carbonate at 100° C. for 5 hours; melting point: 71° C.), dissolved in 200 ml of ethanol, 1.5 g of sodium borohydride was added slowly under stirring at a temperature of max. 30° C. After stirring at room temperature for 6 hours the mixture was evaporated under reduced pressure. The residue was extractively worked up with dilute sodium hydroxide solution and with methylene chloride. The combined methylene chloride phases were washed with water, dried and evaporated under reduced pressure. The residue was purified by means of chromatography on silica gel (mobile phase: methylene chloride/ethanol/ammonia-solution (28%), volume ratio 8:2:0.2) and by recrystallization from methylene chloride/diethylether.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 特許番号 | US05082845 |
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| 出典データセット | uspto-grants-1992_01 |
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| ORD ID | ord-7f5b32a38f7b466daa990c97d7169274 |
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| 出典メモ | uspto-grants-1992_01 |
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