HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1620384Generated: November 1, 2026
HCID 67494711, compound → HCID 67494912, compound
https://huagongshe.com/reaction/1620384
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | HCID 67494711 | HCID 67494711 | — |
| Catalyst | Palladium | HCID 23938 | — |
| Solvent | Acetic Acid | HCID 176 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Solvent | 1,4-Dioxane | HCID 31275 | — |
| Product | HCID 67494912 | HCID 67494912 | 100.9% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08772478B2 |
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| Source dataset | uspto-grants-2014_07 |
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| ORD ID | ord-45228442ef7647c1bf01a98d25e25abe |
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| Source note | uspto-grants-2014_07 |
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