Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Acetic Acid | HCID 176 | — |
| Reactant | HCID 10637170 | HCID 10637170 | — |
| Reactant | (R)-N-(5-(2-amino-1-hydroxyethyl)-2-hydroxyphenyl)methanesulfonamide | HCID 12047933 | — |
| Catalyst | Palladium | HCID 23938 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | HCID 10648298 | HCID 10648298 | 94.2% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06525202B2 |
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| Source dataset | uspto-grants-2003_02 |
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| ORD ID | ord-90ce94ef53294e44948948301ac60d10 |
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| Source note | uspto-grants-2003_02 |
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