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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 448787Generated: October 30, 2026

L-Methionine → N-[[1-[[(4-Methoxyphenyl)carbonyl]amino]cyclohexyl]carbonyl]-L-methionine

https://huagongshe.com/reaction/448787

Reaction equation

Participants

RoleNameHCIDCharge
ReactantL-MethionineHCID 6137—
Reactant2-(4-Methoxyphenyl)-3-oxa-1-azaspiro[4.5]dec-1-en-4-oneHCID 57672857—
Solvent4-MethylmorpholineHCID 7972—
ProductN-[[1-[[(4-Methoxyphenyl)carbonyl]amino]cyclohexyl]carbonyl]-L-methionineHCID 2473801813%

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 heated under reflux 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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08481725B2
Source datasetuspto-grants-2013_07
ORD IDord-7bef9cc9153344d59345a45f617b6327
Source noteuspto-grants-2013_07