関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|
| 反応物 | 1-Bromo-1-propene | HCID 11533 | — |
| 反応物 | Sodium Bicarbonate | HCID 516892 | — |
| 反応物 | 9-[(4-fluorophenyl)methyl]-N-(4-piperidinyl)-9H-purin-8-amine | HCID 19785343 | — |
| 溶媒 | Ethanol | HCID 702 | — |
| 生成物 | 9-[(4-fluorophenyl)methyl]-N-[1-(2-propenyl)-4-piperidinyl)-9H-purin-8-amine | HCID 19785242 | 22% |
反応手順
A mixture of 1.2 parts of bromo-1-propene, 3.26 parts of 9-[(4-fluorophenyl)methyl]-N-(4-piperidinyl)-9H-purin-8-amine, 1.5 parts of sodium hydrogen carbonate and 40 parts of ethanol was stirred for 1 hour at reflux temperature. The reaction mixture was filtered over diatomaceous earth while hot and the filtrate was evaporated. The residue was taken up in water and the product was extracted with 4-methyl-2-pentanone. The extract was dried, filtered and evaporated. The residue was purified by column chromatography over silica gel using a mixture of trichloromethane and methanol, saturated with ammonia, (95:5 by volume) as eluent. The pure fractions were collected and the eluent was evaporated. The residue was crystallized from acetonitrile. The product was filtered off and dried, yielding 0.8 parts (22%) of 9-[(4-fluorophenyl)methyl]-N-[1-(2-propenyl)-4-piperidinyl)-9H-purin-8-amine; mp. 144.8° C. (compound 120).
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 特許番号 | US05258380 |
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| 出典データセット | uspto-grants-1993_11 |
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| ORD ID | ord-6a068b16c7e5448499de677d54ff443f |
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| 出典メモ | uspto-grants-1993_11 |
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