HuagongsheHuagongshe Chemistry Print Report · For research reference only
Triethylamine → HCID 131711691, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | N-[(Phenylmethoxy)carbonyl]-L-leucine 2,5-dioxo-1-pyrrolidinyl ester | HCID 11089751 | — |
| Reactant | HCID 131711685 | HCID 131711685 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | HCID 131711691 | HCID 131711691 | 77.7% |
Reaction Steps
5.0 g (14.0 mmoles) of H-Asp(OtBu)-D-Phg-NH2.HCl, prepared as described in Example 1, Step 4, and 5.13 g (14.2 mmoles) of Z-Leu-OSu are dissolved in 60 ml of DMF, and 1.96 ml (14.0 mmoles) of triethylamine are added to the solution. Next day the reaction mixture is evaporated in vacuo, and the residue is triturated with water. The resulting crude product, weighing 7.32 g, is recrystallized from ethanol under decolourizing. 6.05 g (77.7%) of Z-Leu-Asp(OtBu)-D-Phg-NH2 are obtained; m.p.: 192°-194° C., Rf4 : 0.75. A sample of the product melts as 195°-196° C. after recrystallization from ethanol; [α9 D : -69.5° (c: 1.0, in dimethyl formamide).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04183909 |
| Source dataset | uspto-grants-1980_01 |
| ORD ID | ord-2e3f4c751d6b4e20b69c51ca0a9309cf |
| Source note | uspto-grants-1980_01 |