HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ethylmorpholine → Boc-Tyr-(D)Ala-Gly-MePhe methioninol
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ethylmorpholine | HCID 7525 | — |
| Reactant | Isobutyl chloroformate | HCID 62365 | — |
| Reactant | Boc-tyr-D-ala-gly-OH | HCID 7272028 | — |
| Reactant | H-Tyr-(D)Ala-Gly-Phe methioninol | HCID 131712171 | — |
| Solvent | Acetic Acid | HCID 176 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | Boc-Tyr-(D)Ala-Gly-MePhe methioninol | HCID 131712177 | — |
Reaction Steps
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°.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04261888 |
| Source dataset | uspto-grants-1981_04 |
| ORD ID | ord-e9f243a1c768419ab4f101f624c80188 |
| Source note | uspto-grants-1981_04 |