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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1353176Generated: October 25, 2026

4-Methylmorpholine → Cbz-Dap(Boc)-Ala-OBn

https://huagongshe.com/reaction/1353176

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-MethylmorpholineHCID 7972—
Reactant1-HydroxybenzotriazoleHCID 75771—
Reactantbenzyl (2S)-2-aminopropanoateHCID 726858—
ReactantL-N-Cbz-3-N-Boc-Amino-alanineHCID 2756240—
SolventDichloromethaneHCID 6344—
SolventEthyl AcetateHCID 8857—
ProductCbz-Dap(Boc)-Ala-OBnHCID 131726457—

Reaction Steps

Cbz-Dap(Boc)-OH (0.41 g, 1.2 mmol) was treated with a mixture of 1-(3-(dimethylamino)propyl)-3-ethylcarbodiimide methiodide (0.374 g, 1.26 mmol) and N-hydroxybenzotriazole (0.17 g, 1.26 mmol) in N-methylmorpholine (0.28 mL, 2.1 mmol) in dichloromethane. H-Ala-OBn (0.26 g, 1.2 mmol) was added to the above solution and the resulting mixture was stirred for 14 h at room temperature, then diluted with ethyl acetate (40 mL). The organic solution was washed with 10% aqueous citric acid solution (2×30 mL), saturated aqueous sodium bicarbonate solution (2×30 mL) and brine (2×30 mL). The organic layer was dried over magnesium sulfate and then concentrated in vacuo. The crude compound (247) (0.51 g) was used without further purification.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07220875B2
Source datasetuspto-grants-2007_05
ORD IDord-3d36004113a24f3283193389f5edfbd2
Source noteuspto-grants-2007_05