HuagongsheHuagongshe Chemistry Print Report · For research reference only
Triethylamine → L-Isoleucine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | HCID 21475927 | HCID 21475927 | — |
| Reactant | HCID 86751513 | HCID 86751513 | — |
| Reactant | HCID 178444557 | HCID 178444557 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | L-Isoleucine | HCID 6306 | 25% |
Reaction Steps
Using the procedure described in Example 5, a solution of L-proline-L-isoleucine benzylamide (160 mg, 0.50 mmol), and triethylamine (352 uL, 2.53 mmol, 5.0 eq), in THF (2 mL), was treated with 232 mg (1.0 mmol) of 1-chloro-2-(4-pentylcyclohexyl)-2-oxoethane (prepared from trans-4-pentylcyclohexanecarboxylic acid using the procedure described in example 1) to provide 154 mg, (25%) of L-isoleucine, N-[1-(2-(4-pentylycyclohexyl)-2-oxoethyl)-L-prolyl] benzylamide.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05686424 |
| Source dataset | uspto-grants-1997_11 |
| ORD ID | ord-418d8366bb2f48cda371486bea62d194 |
| Source note | uspto-grants-1997_11 |