HuagongsheHuagongshe Chemistry Print Report · For research reference only
Phenacyl bromide → L-isoleucine, N-[1-(2-phenyl-2-oxoethyl)-L-prolyl] benzylamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Phenacyl bromide | HCID 6259 | — |
| Reactant | Cesium carbonate | HCID 10796 | — |
| Reactant | HCID 86751513 | HCID 86751513 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | L-isoleucine, N-[1-(2-phenyl-2-oxoethyl)-L-prolyl] benzylamide | HCID 67621189 | 94% |
Reaction Steps
Using the procedure described in example 5, treatment of L-proline-L-isoleucine benzylamide (361 mg, 1.14 mmol), with cesium carbonate (0.74 g, 2.28 mmol), and 2-bromoacetophenone (1.134 g, 5.69 mmol, 5.0 eq) in acetonitrile (12 mL), provided 466 mg (94%) of L-isoleucine, N-[1-(2-phenyl-2-oxoethyl)-L-prolyl] benzylamide as a pale yellow oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05686424 |
| Source dataset | uspto-grants-1997_11 |
| ORD ID | ord-1807b6b7496a4fdf8004b42137c63c44 |
| Source note | uspto-grants-1997_11 |