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
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | 4-Morpholinecarbonyl chloride | HCID 84810 | — |
| Reactant | N-[N-[(Phenylmethoxy)carbonyl]-L-leucyl]-L-norleucinol | HCID 15168139 | — |
| Catalyst | HCID 178418390 | HCID 178418390 | — |
| Solvent | Methanol | HCID 887 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | N-[N-(4-Morpholinylcarbonyl)-L-leucyl]-L-norleucinol | HCID 57672829 | 71% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08829209B2 |
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| Source dataset | uspto-grants-2014_09 |
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| ORD ID | ord-670ec47910c144b2a4014bd1f9b264d1 |
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| Source note | uspto-grants-2014_09 |
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