関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|
| 反応物 | Isopropyl iodide | HCID 6362 | — |
| 反応物 | Cesium carbonate | HCID 10796 | — |
| 反応物 | 2-chloro-N-(3-chlorophenyl)-9H-purin-6-amine | HCID 21988232 | — |
| 溶媒 | Ethyl Acetate | HCID 8857 | — |
| 溶媒 | 1,4-Dioxane | HCID 31275 | — |
| 溶媒 | N,N-Dimethylformamide--water (1/1) | HCID 21962138 | — |
| 生成物 | 2-Chloro-N-(3-chlorophenyl)-9-isopropyl-9H-purin-6-amine | HCID 21988248 | — |
反応手順
500 mg (1.78 mmol) of 2-chloro-6-(3-chloro-phenyl-amino)-purine are dissolved in a mixture of 29.5 ml of DMF/water (85/15) and 5 ml of dioxane by means of gentle heating. 870 mg (2.67 mmol) of caesium carbonate, followed by 1.78 ml (17.8 mmol) of isopropyl iodide are added at room temperature. The reaction mixture is stirred at room temperature for 18 hours. To bring the reaction to completion, the reaction mixture is stirred at 45° C. for a further 24 hours. When the reaction has ended, the reaction mixture is diluted with ethyl acetate, washed with water (2 times) and saturated sodium chloride solution and dried over magnesium sulfate. After filtration, the filtrate is concentrated under reduced pressure at 35° C. and the residue is dried under an HV. The resulting crude product is purified by crystallization from diethyl ether/hexane. 2-Chloro-6-(3-chloro-phenyl-amino)-9-isopropyl-9H-purine is obtained; Rf=0.46 (ethyl acetate); m.p. 128–129° C.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 特許番号 | US07091346B1 |
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| 出典データセット | uspto-grants-2006_08 |
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| ORD ID | ord-74fde67f2a9f47cb945db7fa6bea0160 |
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| 出典メモ | uspto-grants-2006_08 |
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