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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 849688Generated: October 30, 2026

4-Methylmorpholine → HCID 12020545, compound

https://huagongshe.com/reaction/849688

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-MethylmorpholineHCID 7972—
ReactantIsobutyl chloroformateHCID 62365—
ReactantBoc-Lys(Z)-OHHCID 2724765—
ReactantL-Leucine, L-leucyl-, methyl ester, hydrochloride (1:1)HCID 15598024—
SolventEthyl AcetateHCID 8857—
ProductHCID 12020545HCID 1202054590.2%

Reaction Steps

Isobutyl chloroformate (13.66 g, 100 mmol) was added dropwise over 15 min at -15 to -10° C. to a solution of Boc-Lys(Z)-OH (38.04 9, 100 mmol) in ethyl acetate (200 g). Another portion of ethyl acetate was added (10 g) and the mixture was stirred for 15 min. 4-Methylmorpholine (10.12 g, 100 mmol) was added dropwise over 15 min at -15 to -10° C., followed by an additional portion of ethyl acetate (10.0 g) and the resulting mixture was stirred for 2 h. In a separate reaction vessel 4-methylmorpholine (10.12 g, 100 mmol) was added dropwise over 15 min, to a solution of H-Leu-Leu-OMe·HCl (29.48 g, 100 mmol) in ethyl acetate (200.0 g) at -23 to -10° C. An additional portion of ethyl acetate (10.0 g) was added followed by the addition of the formed anhydride over 30 to 45 min at a temperature of -8 to -10° C. Another portion of ethyl acetate (30.0 g) was added and the resulting mixture was stirred for 1.5 h. Ethyl acetate (50.00 g) was added, the solution was filtered and the resulting organic filtrate was concentrated in vacuo. The resulting solid was recrystallized from petroleum ether (bp 100 to 125) to give Boc-Lys(Z)-Leu-Leu-OMe (55.9 g, 90.2%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06013764
Source datasetuspto-grants-2000_01
ORD IDord-d1f8416c182e40b0ad394d5b311fcde7
Source noteuspto-grants-2000_01