HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
Dicyclohexylcarbodiimide → Urea
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|---|---|---|
| Edukt | Dicyclohexylcarbodiimide | HCID 10868 | — |
| Edukt | Aminopterin | HCID 169371 | — |
| Edukt | Leu-Ala-Leu-Ala | HCID 53729605 | — |
| Lösungsmittel | Dimethylformamide | HCID 6228 | — |
| Produkt | Urea | HCID 1176 | — |
| Produkt | Aminopterin | HCID 169371 | — |
Reaktionsschritte
Conjugation Via Leu-Ala-Leu-Ala Spacer: The N-hydroxysuccinimide ester of aminopterin was prepared as above. To 10.2 ml of a 23 mM solution of the aminopterin derivative (0,236 mmol) in dimethylformamide were added 104 mg (0,236 mmol) of solid L-Leu-L-Ala-L-Leu-L-Ala (LALA). The mixture was stirred overnight at 50° C. during which time the solid LALA dissolved. To the reaction mixture was added 48.7 mg (0.236 mmol) of dicyclohexylcarbodiimide in 0.58 ml of dimethylformamide. Copious quantities of urea formed within 2 hours at room temperature and were removed by filtration. The filtrate containing the N-hydroxy succinimide ester of the LALA derivative of aminopterin was retained.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patentnummer | US05474765 |
| Quelldatensatz | uspto-grants-1995_12 |
| ORD ID | ord-54fbf15dbc4e4b49a3124476191332a0 |
| Quellennotiz | uspto-grants-1995_12 |