HuagongsheHuagongshe Chemistry Print Report · For research reference only
N-formyl-L-leucine 1-[(trans-3-hexyl-4-oxo-2-oxetanyl)methyl]-4-pentenyl ester → N-formyl-L-leucine 1-[(trans-3-hexyl-4-oxo2-oxetanyl]-methyl]pentyl ester
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | N-formyl-L-leucine 1-[(trans-3-hexyl-4-oxo-2-oxetanyl)methyl]-4-pentenyl ester | HCID 86743995 | — |
| Reactant | HCID 178418361 | HCID 178418361 | — |
| Catalyst | Palladium | HCID 23938 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | N-formyl-L-leucine 1-[(trans-3-hexyl-4-oxo2-oxetanyl]-methyl]pentyl ester | HCID 86743994 | — |
Reaction Steps
A solution of 10 mg of N-formyl-L-leucine 1-[(trans-3-hexyl-4-oxo-2-oxetanyl)methyl]-4-pentenyl ester in 0.5 ml of THF was treated with 2.5 mg of 5% Pd/C and hydrogenated. After the hydrogen uptake was finished the catalyst was filtered off and the filtrate was evaporated in vacuo. The residue was chromatographed over silica gel with toluene/ethyl acetate (8:2) and there was obtained amorphous N-formyl-L-leucine 1-[(trans-3-hexyl-4-oxo-2-oxetanyl]-methyl]pentyl ester as a mixture of 2 diastereomers.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05246960 |
| Source dataset | uspto-grants-1993_09 |
| ORD ID | ord-07a20e79c2184112a21669dbf5ac6d48 |
| Source note | uspto-grants-1993_09 |