HuagongsheHuagongshe Chemistry Print Report · For research reference only
Piperidin-4-ol → HCID 46916505, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Piperidin-4-ol | HCID 79341 | — |
| Reactant | HCID 46916455 | HCID 46916455 | — |
| Solvent | Isopropanol | HCID 3776 | — |
| Product | HCID 46916505 | HCID 46916505 | 26.4% |
Reaction Steps
A mixture of 2-bromo-N-(3-(quinoxalin-2-yl)phenyl)acetamide (93 mg, 0.272 mmol) and 4-hydroxypiperidine (138 mg, 1.35 mmol) in isopropanol (5 mL) was heated at reflux for 1 h. The solvent was evaporated in vacuo and the crude reaction mixture was purified by preparative LCMS to afford 2-(4-hydroxypiperidin-1-yl)-N-(3-(quinoxalin-2-yl)phenyl)acetamide (26 mg, 26% yield). LCMS calculated for C21H22N4O2 (M+H): 363.43. found 363.40. 1H-NMR (CD3CN, 400 Mhz) δH: 9.55 (1H, br.), 9.25 (1H, s), 8.40 (1H, m), 8.00-8.05 (2H, m), 7.85-7.90 (1H, m), 7.65-7.80 (3H, m), 7.40-7.48 (1H, m), 3.65 (1H, m), 3.22 (2H, s), 2.85-3.15 (OH and 2H, br. and m), 2.40-2.50 (2H, m), 1.82-1.92 (2H, m), 1.55-1.68 (2H, m).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08592415B2 |
| Source dataset | uspto-grants-2013_11 |
| ORD ID | ord-2678c8498ee94f8b9f3ed68986f0ba88 |
| Source note | uspto-grants-2013_11 |