関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|
| 反応物 | Ammonia | HCID 222 | — |
| 反応物 | Methanol | HCID 887 | — |
| 反応物 | Bromotrimethylsilane | HCID 76113 | — |
| 反応物 | [4-(7-Ethoxymethyl-3-methylxanthin-1-yl)butyl]phosphonate | HCID 19689210 | — |
| 溶媒 | Dichloromethane | HCID 6344 | — |
| 生成物 | Diammonium [4-(7-ethoxymethyl-3-methylxanthin-1-yl)butyl]phosphonate | HCID 86752277 | — |
反応手順
3.4 ml (0.026 mol) of trimethylsilyl bromide were slowly added dropwise at 0° C., under an argon atmosphere, to a solution of 4.16 g (0.01 mol) of [4-(7-ethoxymethyl-3-methylxanthin-1-yl)butyl]phosphonate in 5 ml of dichloromethane. The solution was stirred at 0° C. for 1 hour and at room temperature for 2 hours. The dichloromethane was then evaporated and the oily residue which remained was dried in a bulb tube in an oil pump vacuum to remove excess trimethylsilyl bromide and ethyl bromide formed. The residue was taken up in a little methanol and treated with 1 ml of concentrated ammonia solution and stirred at room temperature for 2 hours. After evaporating the solvent, the diammonium salt was crystallized from a methanoltdiisopropyl ether mixture.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 特許番号 | US05728686 |
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| 出典データセット | uspto-grants-1998_03 |
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| ORD ID | ord-8959e916559b4ac888f77a67d88387d1 |
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| 出典メモ | uspto-grants-1998_03 |
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