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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1279186Generated: October 26, 2026

4-Methylmorpholine → HCID 178465172, compound

https://huagongshe.com/reaction/1279186

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-MethylmorpholineHCID 7972—
Reactant1-Ethyl-3-(3'-dimethylaminopropyl)carbodiimideHCID 15908—
ReactantN-HydroxysuccinimideHCID 80170—
Reactanttert-Butoxycarbonyl-D-leucineHCID 637604—
ReactantHCID 178465175HCID 178465175—
SolventDimethylformamideHCID 6228—
SolventTetrahydrofuranHCID 8028—
ProductHCID 178465172HCID 17846517292.1%

Reaction Conditions

Temperature0 °C

Reaction Steps

H-Leu-Arg(Tos)-Pro-NHEt was dissolved in 80 mL of DMF and 200 mL of THF. With cooling the solution was neutralized with N-methylmorpholine. To the solution, a solution in which 8.86 g of Boc-D-Leu-OH and 23.02 g of HOSu were dissolved in 200 mL of THF, and 36.4 mL of WSC were added. Next the mixture was stirred at 0° C. for 5 minutes and at room temperature overnight. After confirmation with ninhidrin, the reaction mixture was concentrated under reduced pressure. To the residue, 500 mL of water was added, then the mixture was extracted 5 times with 200 mL of n-butanol and washed five times with water. The n-butanol layer was concentrated under reduced pressure, then the residue was solidified by treatment with ether. Thus 21.5 g of Boc-D-Leu-Leu-Arg(Tos)-Pro-NHEt (92.1% yield) was obtained.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06448031B1
Source datasetuspto-grants-2002_09
ORD IDord-dbb7accad3824ede81c12eda69c1e149
Source noteuspto-grants-2002_09