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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 651828Generated: November 3, 2026

p-Toluenesulfonic acid monohydrate → HCID 86757335, compound

https://huagongshe.com/reaction/651828

Reaction equation

Participants

RoleNameHCIDCharge
Reactantp-Toluenesulfonic acid monohydrateHCID 521998—
ReactantHCID 86757336HCID 86757336—
SolventMethanolHCID 887—
SolventEthyl AcetateHCID 8857—
ProductHCID 86757335HCID 8675733582.9%

Reaction Steps

A solution of 0.045 g of (E)-N-(3-benzyl-2,4,5-trioxo-1-imidazolidinyl]-2(R)-[1(S)-[(tetrahydro-2(RS)-pyranyloxy)carbamoyl]-4-phenyl-3-butenyl]-4-methylvaleramide in 2 ml of methanol was treated with 0.010 g of p-toluenesulphonic acid monohydrate and stirred at room temperature for 2 hours. The mixture was diluted with ethyl acetate and washed in sequence with 5% aqueous sodium hydrogen carbonate and saturated aqueous sodium chloride. The organic layer was dried over anhydrous magnesium sulphate and evaporated to give a residue which was triturated with diethyl ether to give 0.032 g of (E)-N-(3-benzyl-2,4,5-trioxo-1-imidazolidinyl]-2(R)-[1(S)-(hydroxycarbamoyl)-4-phenyl-3-butenyl]-4-methylvaleramide in the form of a white solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06281363B1
Source datasetuspto-grants-2001_08
ORD IDord-3685928975264a56921c3258d02f7338
Source noteuspto-grants-2001_08