HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
Ethylmorpholine → Boc-Tyr-(D)Ala-Gly-MePhe methioninol
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|---|---|---|
| Edukt | Ethylmorpholine | HCID 7525 | — |
| Edukt | Isobutyl chloroformate | HCID 62365 | — |
| Edukt | Boc-tyr-D-ala-gly-OH | HCID 7272028 | — |
| Edukt | H-MePhe methioninol | HCID 131713440 | — |
| Lösungsmittel | Acetic Acid | HCID 176 | — |
| Lösungsmittel | Tetrahydrofuran | HCID 8028 | — |
| Lösungsmittel | H-Tyr-(D)Ala-Gly-Phe methioninol | HCID 131712171 | — |
| Produkt | Boc-Tyr-(D)Ala-Gly-MePhe methioninol | HCID 131712177 | — |
Reaktionsschritte
1.23 g of Boc-Tyr-(D)Ala-Gly-OH is dissolved in 30 ml of THF and cooled to 15°. 0.38 ml of ethylmorpholine are added with stirring followed by 0.39 ml of chloroformic acid iso-butyl ester and stirring continued for 10 minutes. A cold solution of 14 g of TFA.H-MePhe-methioninol and 0.45 ml of N-ethylmorpholine in 12 ml of TFA are added with stirring at -15°. The mixture is stirred for 20 hours at 0°, diluted with 250 ml of acetic acid and washed repeatedly with water, 1 N citric acid, 10% KHCO3 and 30% NaCl solution. The liquid is dried over Na2SO4 and evaporated. The residue is purified chromatographically on kieselgel using a mixture of methanol/CH2Cl2 /50% acetic acid, whereby the title compound is obtained. Decomp. 160°.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patentnummer | US04438103 |
| Quelldatensatz | uspto-grants-1984_03 |
| ORD ID | ord-56049c7444b54325a9f1bc890210a4f4 |
| Quellennotiz | uspto-grants-1984_03 |