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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 651782Generated: October 31, 2026

p-Toluenesulfonic acid monohydrate → HCID 11452605, compound

https://huagongshe.com/reaction/651782

Reaction equation

Participants

RoleNameHCIDCharge
Reactantp-Toluenesulfonic acid monohydrateHCID 521998—
ReactantHCID 11167840HCID 11167840—
SolventMethanolHCID 887—
ProductHCID 11452605HCID 1145260529.7%

Reaction Steps

A solution of 0.280 g of 2(R)-[4-cyclohexyl-1(S)-[(tetrahydro-2(RS)-pyranyloxy)carbamoyl]butyl]-4-methyl-N-(2,5-dioxo-1-imidazolidinyl)valeramide in 10 ml of methanol was treated with 0.028 g of p-toluenesulphonic acid monohydrate. The mixture was stirred for 2 hours at room temperature and evaporated. The residue was dissolved in ethyl acetate, washed with 5% aqueous sodium hydrogen carbonate, dried over anhydrous magnesium sulphate and evaporated. The residue was purified by flash column chromatography on silica gel using methanol/dichloromethane (1:9) for the elution to give 0.069 g of 2(R)-[4-cyclohexyl-1(S)-(hydroxycarbamoyl)butyl]-4-methyl-N-(2,5-dioxo-1-imidazolidinyl)valeramide in the form of a white solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06281363B1
Source datasetuspto-grants-2001_08
ORD IDord-5c71463e7a5c463da7564c19f9439112
Source noteuspto-grants-2001_08