関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|
| 反応物 | Dimethyl Sulfoxide | HCID 679 | — |
| 反応物 | Cysteamine | HCID 6058 | — |
| 反応物 | Sodium hydride | HCID 24758 | — |
| 反応物 | Thiourea dioxide | HCID 61274 | — |
| 反応物 | Sodium | HCID 5360545 | — |
| 反応物 | 2-aminoethanethiol Dihydrochloride | HCID 10154133 | — |
| 反応物 | Sodium Methoxide | HCID 10942334 | — |
| 溶媒 | Methanol | HCID 887 | — |
| 溶媒 | Water | HCID 962 | — |
| 生成物 | 4-(((2-Aminoethyl)thio)methyl)-5-methylimidazole | HCID 665568 | 45% |
反応手順
Triphenyl β-acetylvinylphosphonium bromide (4.11 g, 0.01 mole) was added in one portion to a stirred suspension of 1.1 g (0.01 mole) of formamidine sulfinic acid in 20 ml of dimethylsulfoxide containing 0.25 g of sodium hydride. The mixture was stirred at ambient temperature for 1 hour then at 80° for an additional hour. A solution of 0.99 g (0.01 mole) of the sodium salt of cysteamine, prepared by addition of two equivalents of sodium methoxide to cysteamine dihydrochloride, in 10 ml of methanol was added and the resulting mixture was heated at 70°-80° for 4 hours. The mixture was diluted with twice its volume of water and the triphenyl phosphine was removed by filtration. The filtrate was extracted with 100 ml of toluene and with two 100 ml portions of chloroform. The chloroform extracts were combined, dried and evaporated to dryness to give 4-(2-aminoethyl)thiomethyl-5-methylimidazole in 45% yield.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 特許番号 | US04163858 |
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| 出典データセット | uspto-grants-1979_08 |
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| ORD ID | ord-77e8e0a94005434c9bcf97a7ff593841 |
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| 出典メモ | uspto-grants-1979_08 |
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