HuagongsheHuagongshe Chemistry Print Report · For research reference only
Diisopropyl Ether → HCID 178455965, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Diisopropyl Ether | HCID 7914 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Z-Ile-OSu | HCID 13361528 | — |
| Reactant | H-His-Lys(Boc)-OMe | HCID 178501448 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | HCID 178455965 | HCID 178455965 | — |
Reaction Steps
1.32 g of Z-Ile-OSu [G. W. Anderson et. al., J. Amer. Chem. Soc. 86, 1839 (1964)] are dissolved in the above solution of H-His-Lys(Boc)-OMe in approximately 10 ml of DMF and mixed with 0.41 ml of NEt3. The whole is left to stand for 8 hours at room temperature, 15 ml of diisopropyl ether are added, and the whole is homogenised and filtered. The residue obtained by filtering with suction is dissolved in 15 ml of methanol and added at 0° to 23 ml of aqueous NaHCO3 solution. The resulting precipitate is filtered off, washed with H2O, dried and dissolved and reprecipitated from MeOH/ethyl acetate/petroleum ether, yielding Z-Ile-His-Lys(Boc)-OMe in the form of amorphous powder; Rf (B)=0.65; Rf (I)=0.48.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04595677 |
| Source dataset | uspto-grants-1986_06 |
| ORD ID | ord-ce8789a81b9d458eb11bf86f4f86ebac |
| Source note | uspto-grants-1986_06 |