HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
S-benzyl-L-cysteine → N-carbamyl-S-benzylcysteine
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|---|---|---|
| Edukt | S-benzyl-L-cysteine | HCID 193613 | — |
| Edukt | Potassium cyanate | HCID 11378442 | — |
| Produkt | N-carbamyl-S-benzylcysteine | HCID 57148047 | — |
Reaktionsschritte
The desired compound was synthesized from S-benzyl-L-cysteine (2 g, 9.48 mmol) (Fluka) and potassium cyanate (1.7 g, 21 mmol) by a modification of published protocols [see Coll. Czech Chem. Commun. 33:2918 (1968)]. Instead of isolating the N-carbamyl-S-benzylcysteine intermediate, after an initial reflux of 1 h, 25 ml of 10% hydrochloric acid was added and reflux was continued for 1.5 h. Upon cooling, the desired product precipitated as a white solid 1.7 g (77% yield), melting point 119.5°-120.5° C.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patentnummer | US05767140 |
| Quelldatensatz | uspto-grants-1998_06 |
| ORD ID | ord-c6bdfad1771c4459b3c1bd5e0e7d25e7 |
| Quellennotiz | uspto-grants-1998_06 |