関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|
| 反応物 | Methanol | HCID 887 | — |
| 反応物 | Carbon Disulfide | HCID 6348 | — |
| 反応物 | 5-amino-1-beta-D-ribofuranosylimidazole-4-carboxamide O-ethyl-oxime | HCID 53763093 | — |
| 生成物 | 2-Thioadenosine | HCID 6451965 | — |
反応手順
0.45 g of 5-amino-1-β-D-ribofuranosylimidazole-4-carboxamide O-ethyl-oxime was dissolved in 8 ml of an aqueous solution containing 7 ml of methanol, and 2 ml of carbon disulfide was added to the solution. The resulting mixture was allowed to react in an autoclave at 120° C for 6 hours under autogenous pressure (about 10 Kg/cm2). The reaction mixture was concentrated to dryness, and the residue was dissolved in water. The aqueous solution was adjusted to a pH of 2 with hydrochloric acid, and the crystals thus precipitated were filtered to obtain 2-thioadenosine, which was then dissolved in aqueous ammonia, filtered and again adjusted to a pH of 2 with hydrochloric acid to obtain 0.355 g of pure 2-thioadenosine having a melting point of 199° C (with decomposition) in a 75% yield.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 特許番号 | US03989682 |
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| 出典データセット | uspto-grants-1976_11 |
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| ORD ID | ord-75e78e4fc27e4e2cb3ac6078bb8e2e6a |
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| 出典メモ | uspto-grants-1976_11 |
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