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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1627496Generated: November 3, 2026

L-Methionine → N-[[1-[(2-Benzothienylcarbonyl)amino]cyclohexyl]carbonyl]-L-methionine

https://huagongshe.com/reaction/1627496

Reaction equation

Participants

RoleNameHCIDCharge
ReactantL-MethionineHCID 6137—
Reactant2-(2-Benzothienyl)-3-oxa-1-azaspiro[4.5]dec-1-en-4-oneHCID 57672854—
Solvent4-MethylmorpholineHCID 7972—
ProductN-[[1-[(2-Benzothienylcarbonyl)amino]cyclohexyl]carbonyl]-L-methionineHCID 2473802222.4%

Reaction Steps

10 ml of N-methylmorpholine was added to 522 mg (3.5 mmol) of L-methionine and 500 mg (1.75 mmol) of 2-(2-benzothienyl)-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 sulfate, 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 170 mg (22%) of the title compound.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08785631B2
Source datasetuspto-grants-2014_07
ORD IDord-a4d278ef7b974fcc83d22368e5ca7270
Source noteuspto-grants-2014_07