HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1851859Generated: November 2, 2026
L-Methionine → N-[[1-[[(4-Methoxyphenyl)carbonyl]amino]cyclohexyl]carbonyl]-L-methionine
https://huagongshe.com/reaction/1851859
Participants
| Role | Name | HCID | Charge |
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| Reactant | L-Methionine | HCID 6137 | — |
| Reactant | 2-(4-Methoxyphenyl)-3-oxa-1-azaspiro[4.5]dec-1-en-4-one | HCID 57672857 | — |
| Solvent | 4-Methylmorpholine | HCID 7972 | — |
| Product | N-[[1-[[(4-Methoxyphenyl)carbonyl]amino]cyclohexyl]carbonyl]-L-methionine | HCID 24738018 | 13% |
Reaction Steps
10 ml of N-methylmorpholine was added to 298 mg (2 mmol) of L-methionine and 259 mg (1 mmol) of 2-(4-methoxyphenyl)-3-oxa-1-azaspiro[4.5]dec-1-en-4-one, and the mixture was stirred and refluxed under heating overnight. The reaction solution was distilled off under reduced pressure, a 10% aqueous potassium hydrogensulfate solution was added thereto, and the mixture was extracted with methylene chloride three times. The obtained organic layer was dried with anhydrous sodium hydrogensulfate and the solvent was distilled off under reduced pressure. Ethyl acetate was added to the obtained residue, and the mixture was stirred overnight. The precipitated solid was collected by filtration and dried under reduced pressure to obtain 52 mg (13%) of the title compound.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08957205B2 |
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| Source dataset | uspto-grants-2015_02 |
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| ORD ID | ord-d0457b863b8d4369b6b48fd13fb52e83 |
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| Source note | uspto-grants-2015_02 |
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