HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
Acetaldehyde → Netilmicin
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|---|---|---|
| Edukt | Acetaldehyde | HCID 177 | — |
| Edukt | Hydrochloric Acid | HCID 313 | — |
| Edukt | Nitric Acid | HCID 944 | — |
| Edukt | Phosphoric Acid | HCID 1004 | — |
| Edukt | Sulfuric Acid | HCID 1118 | — |
| Edukt | p-Toluenesulfonic acid | HCID 6101 | — |
| Edukt | Trifluoroacetic acid | HCID 6422 | — |
| Edukt | Sisomicin | HCID 36119 | — |
| Edukt | Sodium cyanoborohydride | HCID 5003444 | — |
| Lösungsmittel | Acetic Acid | HCID 176 | — |
| Lösungsmittel | Water | HCID 962 | — |
| Produkt | Netilmicin | HCID 441306 | — |
Reaktionsschritte
in the procedure of above Example 1A instead of adding 1 N sulfuric acid to the solution of sisomicin in water until it reaches a pH of about 5, other acids may be used, such as acetic acid, trifluoroacetic acid, p-toluenesulfonic acid, hydrochloric acid, phosphoric acid, or nitric acid. The acidified aqueous solution is then treated with acetaldehyde and sodium cyanoborohydride and the resultant product is purified as described above, whereby is obtained 1-N-ethylsisomicin.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patentnummer | US04002742 |
| Quelldatensatz | uspto-grants-1977_01 |
| ORD ID | ord-1cf3e61ee5494d7a91ba96e414aab62f |
| Quellennotiz | uspto-grants-1977_01 |