HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
Phenylalanine amide → N-(toluene-4-sulfonyl)-L-prolyl-L-phenylalanine amide
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|---|---|---|
| Edukt | Phenylalanine amide | HCID 445694 | — |
| Edukt | (2S)-1-(4-methylbenzenesulfonyl)pyrrolidine-2-carboxylic acid | HCID 691957 | — |
| Produkt | N-(toluene-4-sulfonyl)-L-prolyl-L-phenylalanine amide | HCID 54382446 | — |
Reaktionsschritte
N-(Toluene-4-sulfonyl)-L-proline was reacted with L-phenylalanine amide using the procedure described in Method 12 to yield N-(toluene-4-sulfonyl)-L-prolyl-L-phenylalanine amide. To a solution of NaH (60% mineral oil—prewashed with THF) in THF at 0° C. was added N-(toluene-4-sulfonyl)-L-prolyl-L-phenylalanine amide and the reaction was stirred at 0° C. for 45 minutes. Toluene-4-sulfonyl chloride was added and the reaction was stirred for 16 hours at room temperature. The reaction mixture was extracted with EtOAc (3×50 mL) and 0.2 N HCl (50 mL), and the combined organic layers were washed successively with sat. NaHCO3 (50 mL), and sat. NaCl (2×50 mL), dried over MgSO4, filtered, and concentrated to yield the title compound as an oil.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patentnummer | US06362341B1 |
| Quelldatensatz | uspto-grants-2002_03 |
| ORD ID | ord-67481f61b200442a879954aab9626e59 |
| Quellennotiz | uspto-grants-2002_03 |