HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1061309Generated: November 2, 2026
Sodium Bicarbonate → {4-[(2R)-2-Hydroxy-2-(4-hydroxy-3-methanesulfonylamino-phenyl)-ethylamino]-piperidin-1-yl}-benzoic acid ethyl ester
https://huagongshe.com/reaction/1061309
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Reactant | Sodium triacetoxyborohydride | HCID 5049666 | — |
| Reactant | (R)-N-(5-(2-amino-1-hydroxyethyl)-2-hydroxyphenyl)methanesulfonamide | HCID 12047933 | — |
| Reactant | Ethyl 4-(4-oxopiperidin-1-yl)benzoate | HCID 12717442 | — |
| Solvent | Acetic Acid | HCID 176 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | {4-[(2R)-2-Hydroxy-2-(4-hydroxy-3-methanesulfonylamino-phenyl)-ethylamino]-piperidin-1-yl}-benzoic acid ethyl ester | HCID 69654607 | 50% |
Reaction Steps
1-(4-Ethoxycarbonylphenyl)-4-piperidone (Taylor, E. C., Skotnicki, J. S. Synthesis, 1981, 606) (0.29 g, 1.2 mmol) and N-[5-(2-amino-(1R)-1-hydroxy-ethyl)-2-hydroxy-phenyl]-methanesulfonamide (which was obtained in Example 10) (0.29 g, 1.2 mmol) were mixed in dimethylformamide (10 mL) and then treated with sodium triacetoxyborohydride (1.01 g, 4.7 mmol) and acetic acid (0.5 mL). After stirring at room temperature under a nitrogen atmosphere for 15 hours the mixture was poured into a saturated aqueous sodium bicarbonate. The precipitate which was formed was collected and purified by silica gel chromatography (methanol/methylene chloride) to give the titled compound as a white solid (0.28 g, 50%); mp >95° C. (decomposed); 1H NMR (300 MHz, DMSO-d6) δ 1.28 (t, J=7.1 Hz, 3H), 1.30-1.55 (m, 2H), 1.80-1.95 (m, 2H), 2.55-3.50 (m, 5H), 2.92 (s, 3H), 3.75-3.90 (m, 2H), 4.22 (q, J=7.1 Hz, 2H), 6.82 (d, J=8.2Hz, 1H), 6.95 (d, J=8.9Hz, 2H), 7.00 (dd, J=8.2, 1.9Hz, 1H), 7.18 (d, J=1.9 Hz, 1H), 7.75 (d, J=8.9 Hz, 2H); MS (ES) m/z: 478.0 (MH+); HRMS Calcd. for C23H32N3O6S(MH+): 478.2006. Found: 478.2000.
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-28fff3b780224bea8eb9d10e2aad63dc |
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| Source note | uspto-grants-2003_02 |
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