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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1383742Generated: November 2, 2026

4-Methylmorpholine → Z-N-Me-Val-N-Me-Tyr(3-tBu)-NH2

https://huagongshe.com/reaction/1383742

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-MethylmorpholineHCID 7972—
ReactantZ-N-Me-Val-N-Me-Tyr(3-tBu)-OHHCID 131722750—
SolventTetrahydrofuranHCID 8028—
SolventEthyl chloroformateHCID 10928—
ProductZ-N-Me-Val-N-Me-Tyr(3-tBu)-NH2HCID 131722751—

Reaction Steps

To a solution of 1.96 g of Z-N-Me-Val-N-Me-Tyr(3-tBu)-OMe in 1,4-dioxane (40 ml), 2 N NaOH (5 ml) was added at room temperature and the mixture was stirred for 2 hours. The reaction mixture was adjusted to pH 3 with dilute hydrochloric acid and extracted with ethyl acetate. The extract was washed with saturated brine and the organic layer was dried with sodium sulfate. The solvent was distilled off under reduced pressure to give Z-N-Me-Val-N-Me-Tyr(3-tBu)-OH. To a solution of this Z-N-Me-Val-N-Me-Tyr(3-tBu)-OH in THF (20 ml), ethyl chloroformate (0.40 ml) and NMM (0.46 ml) were added under cooling with ice and the mixture was stirred for 15 minutes. Subsequently, ammonia gas was bubbled into the reaction mixture for 5 minutes. The solvent was distilled off under reduced pressure and the precipitating salt was filtered off and washed with ethyl acetate. The solvent was distilled off under reduced pressure and the resulting residue was subjected to silica gel column chromatography (eluting solvent; n-hexane:ethyl acetate=2:3) to give Z-N-Me-Val-N-Me-Tyr(3-tBu)-NH2 in the amount of 1.17 g (61%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06255285B1
Source datasetuspto-grants-2001_07
ORD IDord-6c162120214b404eaacf787832fd716b
Source noteuspto-grants-2001_07