Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 982867Generated: October 30, 2026

Cysteamine → 4-Hydroxy-3-[7-(2-methoxy-4-methylsulfanyl-phenyl)-2,3,6,7-tetrahydro-[1,4]thiazepin-5-yl]-6-methyl-pyran-2-one

https://huagongshe.com/reaction/982867

Reaction equation

Participants

RoleNameHCIDCharge
ReactantCysteamineHCID 6058—
Reactant4-Hydroxy-3-[(E)-3-(2-methoxy-4-methylsulfanyl-phenyl)-acryloyl]-6-methyl-pyran-2-oneHCID 135621892—
SolventEthanolHCID 702—
Product4-Hydroxy-3-[7-(2-methoxy-4-methylsulfanyl-phenyl)-2,3,6,7-tetrahydro-[1,4]thiazepin-5-yl]-6-methyl-pyran-2-oneHCID 13552949141.6%

Reaction Conditions

Temperature80 °C

Reaction Steps

4-Hydroxy-3-[(E)-3-(2-methoxy-4-methylsulfanyl-phenyl)-acryloyl]-6-methyl-pyran-2-one (41.8 mg, 0.126 mmol), prepared as in Reference 5, Step 5.1, was dissolved in absolute ethanol (5 mL) and then 2-aminoethanethiol (9.8 mg, 0.126 mmol) was added to the solution. The mixture was stirred at 80° C. The progress of the reaction was followed by analytical HPLC and when complete (approximately 12 hours) the solvent was removed in vacuo. Product was purified by silica flash column chromatography to provide 4-hydroxy-3-[7-(2-methoxy-4-methylsulfanyl-phenyl)-2,3,6,7-tetrahydro-[1,4]thiazepin-5-yl]-6-methyl-pyran-2-one (20.5 mg) as a pale, yellow solid. LCMS: MH+ 392.6.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06861419B2
Source datasetuspto-grants-2005_03
ORD IDord-d51a8ea00f0d4dfb80a9107b8abdcaed
Source noteuspto-grants-2005_03