HuagongsheHuagongshe Chemistry Print Report · For research reference only
p-Toluenesulfonic acid → (S)-2-[(azepane-1-carbonyl)-amino]-4-methyl-pentanoic acid benzyl ester
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | p-Toluenesulfonic acid | HCID 6101 | — |
| Reactant | Azepane | HCID 8119 | — |
| Reactant | 1,1'-Carbonyldiimidazole | HCID 68263 | — |
| Reactant | Benzyl L-leucinate | HCID 6451313 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | (S)-2-[(azepane-1-carbonyl)-amino]-4-methyl-pentanoic acid benzyl ester | HCID 10593708 | — |
Reaction Steps
TEA (0.73 ml) was added dropwise to a suspension of Leu-OBzl.TsOH (1.97 g) and CDI (0.85 g) in THF (10 ml) at 0°~5° C. over a period of 5 min and the mixture was stirred at the same temperature for 1 h. Perhydroazepine (0.67 ml) was added and the reaction mixture was stirred at room temperature for 14 h, and poured into water (100 ml). The resulting precipitate was collected by filtration to afford the product (1.75 g).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05444152 |
| Source dataset | uspto-grants-1995_08 |
| ORD ID | ord-957f1f73c53048e194808307acf1c919 |
| Source note | uspto-grants-1995_08 |