HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 849694Generated: October 30, 2026
4-Methylmorpholine → Z-Lys(Z)-Leu-Leu-OMe
https://huagongshe.com/reaction/849694
Participants
| Role | Name | HCID | Charge |
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| Reactant | 4-Methylmorpholine | HCID 7972 | — |
| Reactant | Dicyclohexylcarbodiimide | HCID 10868 | — |
| Reactant | 1-Hydroxybenzotriazole | HCID 75771 | — |
| Reactant | N2,N6-Bis[(phenylmethoxy)carbonyl]-L-lysine | HCID 7269422 | — |
| Reactant | L-Leucine, L-leucyl-, methyl ester, hydrochloride (1:1) | HCID 15598024 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | Z-Lys(Z)-Leu-Leu-OMe | HCID 12020551 | 99.7% |
Reaction Steps
4-Methylmorpholine (1.26 g, 12.5 mmol) and HOBt (1.69 g, 12.5 mmol) were added to a solution of H-Leu-Leu-OMe·HCl (4.04 g, 13.75 mmol) in ethyl acetate (160.0 g) and DMF (36.0 g) over 15 min. Z-Lys(Z)-OH (5.18 g, 12.5 mmol) was added to this stirred mixture over 15 min. A solution of DCC (3.10 g, 12.5 mmol) in ethyl acetate (10.0 g) was added dropwise at 18-20° C. over 30 min. The reaction mixture was stirred at 18-20° C. for 16 h and filtered. The filter cake was washed with ethyl acetate (100.0 g) and the combined filtrate was washed with aqueous NaHCO3. The resulting organic layer was washed with aqueous NaCl and concentrated under reduced pressure. The residue was dissolved in MeOH (80.0 g) at about 50° C. Water (160 g) was slowly added and the mixture was stirred for about 1 h at 20° C. The resulting solid was filtered, washed with H2O (80.0 g) and dried at 40° C. in a vacuum oven to give 8.16 g, 99.6% of the product Z-Lys(Z)-Leu-Leu-OMe.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06013764 |
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| Source dataset | uspto-grants-2000_01 |
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| ORD ID | ord-8dba8592b39c4c75b361172b82f4951b |
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| Source note | uspto-grants-2000_01 |
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