化工社化工社 化学情報印刷レポート · 研究参考用
2-Methyl-2-thiopseudourea → neomycin B gamma-guanidino butyric acid
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|---|---|---|
| 反応物 | 2-Methyl-2-thiopseudourea | HCID 5142 | — |
| 反応物 | O-Methylisourea | HCID 75544 | — |
| 反応物 | neomycin B gamma-amino butyric acid | HCID 131724201 | — |
| 溶媒 | Water | HCID 962 | — |
| 生成物 | neomycin B gamma-guanidino butyric acid | HCID 178512978 | — |
反応手順
For guanylation, the neomycin B/γ-amino butyric acid conjugate obtained in Example 9a above is treated with O-methyl isourea or S-methyl isothiourea in water at basic pH for 34 days, resulting in guanylation of the terminal amino groups. The product is purified by ion exchange chromatography, yielding the neomycin B/γ-guanidino butyric acid conjugate 17.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 特許番号 | US06642365B1 |
| 出典データセット | uspto-grants-2003_11 |
| ORD ID | ord-c6f4edae96e8479896f6d399ccd53340 |
| 出典メモ | uspto-grants-2003_11 |