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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 73848Generated: October 29, 2026

Triethylamine → N-[N-(4-Morpholinylcarbonyl)-L-leucyl]-L-norleucinol

https://huagongshe.com/reaction/73848

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
Reactant4-Morpholinecarbonyl chlorideHCID 84810—
ReactantN-[N-[(Phenylmethoxy)carbonyl]-L-leucyl]-L-norleucinolHCID 15168139—
CatalystHCID 178418390HCID 178418390—
SolventMethanolHCID 887—
SolventDichloromethaneHCID 6344—
ProductN-[N-(4-Morpholinylcarbonyl)-L-leucyl]-L-norleucinolHCID 5767282971%

Reaction Steps

70 mg of 10% palladium-carbon was added to a solution of 700 mg (2 mmol) of N—[N-[(phenylmethoxy)carbonyl]-L-leucyl]-L-norleucinol obtained in Reference Example 185 in 10 ml of methanol, and the mixture was stirred under a hydrogen atmosphere at room temperature overnight. After the reaction solution was filtered, the filtrate was concentrated under reduced pressure. 20 ml of methylene chloride and 404 mg (4 mmol) of triethylamine were added to the residue. Under ice-cooling, a solution of 299 mg (2 mmol) of 4-morpholinecarbonyl chloride in 3 ml of methylene chloride was added to the mixture solution. The reaction solution was returned to room temperature and was stirred overnight. After the reaction solution was washed with water and then saturated brine, it was dried with anhydrous sodium sulfate and the solvent was distilled off under reduced pressure. Ether was added to the residue to wash it to obtain 488 mg (71%) of the title compound.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08829209B2
Source datasetuspto-grants-2014_09
ORD IDord-670ec47910c144b2a4014bd1f9b264d1
Source noteuspto-grants-2014_09