関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|
| 反応物 | Taurine | HCID 1123 | — |
| 反応物 | Paclitaxel Succinate | HCID 25024567 | — |
| 溶媒 | Pyridine | HCID 1049 | — |
| 生成物 | Succinic anhydride | HCID 7922 | — |
| 生成物 | Paclitaxel | HCID 36314 | — |
| 生成物 | Paclitaxel Succinate | HCID 25024567 | — |
反応手順
2'-{[4-((2-sulfoethyl)amino)-1,4-dioxobutyl]oxy}taxol sodium salt and 2'-{[4-((3-sulfopropyl)amino-1,4-dioxobutyl]-oxy}taxol sodium salt were produced in high yield by coupling 2'-succinyltaxol with taurine (2-aminoethyl sulfonic acid) and 3-aminopropyl sulfonic acid tetrabutylammonium salts, respectively. Note that other quaternary ammonium salts may be used to make the aminoalkyl sulfonic acids organic solvent soluble. 2'-succinyltaxol was formed by the reaction of succinic anhydride with taxol for two hours at room temperature in pyridine or DMP. In comparison with the NMR spectrum of taxol, the NMR spectrum of 2'-succinyltaxol showed a downfield shift of the C-2' proton signal to 5.51 ppm, and the succinyl proton caused multiplets centered about 2.6 ppm.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| 特許番号 | US05059699 |
|---|
| 出典データセット | uspto-grants-1991_10 |
|---|
| ORD ID | ord-f1b9b1b1b7414784b308a6e5af160e9b |
|---|
| 出典メモ | uspto-grants-1991_10 |
|---|