HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 412083Generated: October 29, 2026
Leucine, N-carboxy-, N-benzyl ester, L- → Z-Leu-Leu methyl ester
https://huagongshe.com/reaction/412083
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Leucine, N-carboxy-, N-benzyl ester, L- | HCID 74840 | — |
| Reactant | 1-Hydroxybenzotriazole | HCID 75771 | — |
| Reactant | Leucine methyl ester hydrochloride | HCID 2723695 | — |
| Reactant | 1,3-Propanediamine, N'-(ethylcarbonimidoyl)-N,N-dimethyl-, monohydrochloride | HCID 2723939 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | Z-Leu-Leu methyl ester | HCID 7237624 | 66% |
Reaction Steps
N-Cbz-L-leucine (Chemical Dynamics) (1.32 g, 4.97 mmol), L-leucine methyl ester hydrochloride (Aldrich) (0.99 g, 5.47 mmol), 1-hydroxybenzotriazole (0.14 g, 1.0 mmol) and 1-(3-dimethylaminopropyl)-3ethylcarbodiimide hydrochloride (1.05 g, 5.47 mmol) were combined, dissolved in 25 nL of DMF and stirred at room temperature for 15 h. The solution was diluted with ethyl acetate (250 mL) and washed successively with water, 0.1 N HCl, saturated aqeous NaHCO3 and saturated brine, then dried (MgSO4), filtered, and concentrated. The residue was purified by flash chromatography on 230-400 mesh silica gel, eluting with 1:3 ethyl acetate hexanes, to give the title compound as a white solid (1.28 g, 66%). 1H NMR (400 MHz, CDCl3) δ 7.37-7.32 (m, 5H), 6.28 (d, 1H), 5.28 (m, 3H), 4.61-4.58 (m, 1H), 4.20 (m, 1H), 3.74 (s, 3H), 1.69-1.54 (m, 6H), 0.96-0.92 (m, 12H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US06562842B2 |
|---|
| Source dataset | uspto-grants-2003_05 |
|---|
| ORD ID | ord-cfebe31312c0463e94270ed374fce100 |
|---|
| Source note | uspto-grants-2003_05 |
|---|