HuagongsheHuagongshe Chemistry Print Report · For research reference only
Triethylamine → HCID 131717864, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | (4S)-4-amino-5-benzyloxy-5-oxo-pentanoic acid | HCID 7009632 | — |
| Reactant | Boc-Thr(Bzl)-OSu | HCID 12879029 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | HCID 131717864 | HCID 131717864 | 87.2% |
Reaction Steps
To a solution of 2.83 g of H-Glu-OBzl dissolved in 40 ml of acetonitrile were added 3.3 ml of triethylamine and 5.00 g of Boc-Thr(Bzl)-OSu under ice-cooling. The mixture was stirred overnight at room temperature. The reaction mixture was concentrated under reduced pressure. The residue was dissolved in 50 ml of ethyl acetate and the resulting solution was washed with 30 ml of water twice. The ethyl acetate layer was dried with anhydrous magnesium sulfate. The solvent was removed by distillation to dry the ethyl acetate layer, whereby 5.50 g (yield: 87.2%) of the above objective compound was obtained as a powder form product.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05204326 |
| Source dataset | uspto-grants-1993_04 |
| ORD ID | ord-0c5d9703500a43a5b5b338648344c05e |
| Source note | uspto-grants-1993_04 |