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Dimethylformamide → 2-Thioadenosine
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|---|---|---|
| 反応物 | Dimethylformamide | HCID 6228 | — |
| 反応物 | Carbon Disulfide | HCID 6348 | — |
| 反応物 | 5-amino-1-beta-D-ribofuranosylimidazole-4-carboxamide O-cyclohexyl-oxime | HCID 54291096 | — |
| 生成物 | 2-Thioadenosine | HCID 6451965 | 76% |
反応手順
0.45 g of 5-amino-1-β-D-ribofuranosylimidazole-4-carboxamide O-cyclohexyl-oxime was dissolved in 4 ml of an aqueous solution containing 3 ml of N,N-dimethylformamide, and 1 ml of carbon disulfide was added to the solution. The resulting mixture was allowed to react in an autoclave at 125° C for 5 hours under autogenous pressure (about 10 Kg/cm2), and the reaction product was worked up in the same manner as described in Example 1 to obtain 0.305 g of 2-thioadenosine having a melting point of 197° C (with decomposition) in 76% yield.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 特許番号 | US03989682 |
| 出典データセット | uspto-grants-1976_11 |
| ORD ID | ord-e41d7a30a3f64cfc888dab9e8e25555e |
| 出典メモ | uspto-grants-1976_11 |