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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1620384Generated: November 1, 2026

HCID 67494711, compound → HCID 67494912, compound

https://huagongshe.com/reaction/1620384

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHCID 67494711HCID 67494711—
CatalystPalladiumHCID 23938—
SolventAcetic AcidHCID 176—
SolventEthyl AcetateHCID 8857—
Solvent1,4-DioxaneHCID 31275—
ProductHCID 67494912HCID 67494912100.9%

Reaction Steps

A solution of 4.9 g (11 mmol) of methyl(S)-3-(4-benzyloxybenzenesulfonylamino)-2-piperidin-1-yl-propanoate (prepared as described in 1.5) in 80 ml of ethyl acetate, 30 ml of dioxane and 0.5 ml of glacial acetic acid is degassed under nitrogen for 15 min and then a suspension of 490 mg (10% by weight) of palladium on carbon at 10% in 3 ml of dioxane is added. The reaction medium is then placed under a hydrogen atmosphere and stirred at ambient temperature for 5 h. After filtration through celite, the filtrate is concentrated under vacuum. The residue is taken up in ethyl acetate, washed with water, dried over magnesium sulfate, filtered and concentrated. 3.8 g (97%) of methyl (S)-3-(4-hydroxybenzenesulfonylamino)-2-piperidin-1-ylpropanoate are obtained in the form of a white solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08772478B2
Source datasetuspto-grants-2014_07
ORD IDord-45228442ef7647c1bf01a98d25e25abe
Source noteuspto-grants-2014_07