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Ammonia → 5-Bromo-2'-deoxyuridine
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|---|---|---|
| 反応物 | Ammonia | HCID 222 | — |
| 反応物 | Triphenylphosphine | HCID 11776 | — |
| 反応物 | Chloroform methanol | HCID 21584188 | — |
| 反応物 | 5'-Azido-5-bromo-2'-deoxyuridine | HCID 54449921 | — |
| 溶媒 | Pyridine | HCID 1049 | — |
| 溶媒 | p-Toluenesulfonic acid | HCID 6101 | — |
| 生成物 | 5-Bromo-2'-deoxyuridine | HCID 6035 | — |
反応手順
The 5'-azido derivative of 5-bromo-2'-deoxy uridine is prepared via the method described above. The 5'-azido-5-bromo-2'-deoxyuridine (1 mmol) is treated with triphenyl phosphine (1.5 mmol) in pyridine at room temperature for 2 h. Concentrated ammonia (1 ml) is added to the reaction vessel. After 14 h the solvent is removed under vacuum. The residue is dissolved in chloroform/ methanol containing one equivalent of p-toluene sulfonic acid, and this solution is added to hexanes. The 5'-amino-5-bromo-2'-deoxyuridine precipitate is collected and dried.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 特許番号 | US05142047 |
| 出典データセット | uspto-grants-1992_08 |
| ORD ID | ord-3ebc1fb9652a4613aadd82a2a585249c |
| 出典メモ | uspto-grants-1992_08 |