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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 448786Generated: October 30, 2026

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

https://huagongshe.com/reaction/448786

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 numberUS08481725B2
Source datasetuspto-grants-2013_07
ORD IDord-55d15a036d1842e1b5eb6950bcb4699a
Source noteuspto-grants-2013_07