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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1061312Generated: November 4, 2026

Acetic Acid → HCID 10648298, compound

https://huagongshe.com/reaction/1061312

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AcidHCID 176—
ReactantHCID 10637170HCID 10637170—
Reactant(R)-N-(5-(2-amino-1-hydroxyethyl)-2-hydroxyphenyl)methanesulfonamideHCID 12047933—
CatalystPalladiumHCID 23938—
SolventMethanolHCID 887—
ProductHCID 10648298HCID 1064829894.2%

Reaction Steps

A solution of (E)-3-[4-(4-oxo-piperidine-1-yl)-phenyl]-acrylic acid (which was obtained in Example 170) (0.10 g, 0.40 mmol) and N-[5-((1R)-2-Amino-1-hydroxy-ethyl)-2-hydroxy-phenyl]-methane-sulfonamide (which was obtained in Example 10) (0.12 g, 0.48 mmol) in methanol (15 mL) was treated with acetic acid (0.03 g, 0.5 mmol), and 0.05 g of 10% Pd/C. The mixture was hydrogenated at 25 psi for 24 h, and then filtered through Celite and evaporated. The residue was triturated with ether to give 0.18 g of an off-white solid; m.p. 130-133° C.; 1H NMR (DMSO-d6) δ 1.30-1.46 (m, 2H), 1.84-1.95 (m, 2H), 2.37-2.50 (m, 4H), 2.60-2.78 (m, 4H), 2.92 (s, 3 H), 3.53-3.62 (m, 3H), 4.46-4.55 (m, 1H), 6.85 (d, 2H), 6.92-7.10 (m, 4H), 7.18 (dd, 1H); MS (ES) m/z: 478.3 (MH+).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06525202B2
Source datasetuspto-grants-2003_02
ORD IDord-90ce94ef53294e44948948301ac60d10
Source noteuspto-grants-2003_02