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2-Chloroadenosine → 2-Thioadenosine
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|---|---|---|
| 反応物 | 2-Chloroadenosine | HCID 8974 | — |
| 反応物 | Sodium hydrogen sulphide | HCID 86586439 | — |
| 溶媒 | Dimethylformamide | HCID 6228 | — |
| 生成物 | 2-Thioadenosine | HCID 6451965 | 100% |
反応手順
The starting material, the 2-thioadenosine of the formula (IV), used in the above Process 2 can be obtained in high yield from 2-chloroadenosine of the formula (II) by the procedure disclosed in Japanese Patent Application OPI No. 52,795/1973. That is, 2-chloroadenosine is reacted with sodium hydrogen sulfide in a solvent such as dimethylformamide at a temperature of about 50°C to 100°C to obtain the desired 2-thioadenosine of the formula (IV) in about 100% yield. The preparation of the starting material of the formula (IV) will be hereinafter described in greater detail in Reference Example 2.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 特許番号 | US03968102 |
| 出典データセット | uspto-grants-1976_07 |
| ORD ID | ord-c4bf991a73df41749e41cb2ca6be71d4 |
| 出典メモ | uspto-grants-1976_07 |