HuagongsheHuagongshe Chemistry Print Report · For research reference only
Piperidin-4-ol → HCID 178515223, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Piperidin-4-ol | HCID 79341 | — |
| Reactant | HCID 178515218 | HCID 178515218 | — |
| Reactant | HCID 178515226 | HCID 178515226 | — |
| Product | HCID 178515223 | HCID 178515223 | — |
Reaction Steps
The title compound was prepared following the procedure described in the synthesis of 28a using 27a and 4-hydroxypiperidine. 1H-NMR (DMSO-d6) δ (ppm): 1.54 (2H, brm), 1.87 (2H, brm), 2.85 (2H, brm), 3.20 (1H, m), 3.64 (1H, brm), 4.74 (1H, brd, J=3.84 Hz), 7.10 (1H, m), 7.22 (1H, d, J=7.97 Hz), 7.40 (2H, m), 7.76 (1H, d, J=2.90 Hz), 8.20 (2H, m), 8.64 (1H, s). m/z 379.2 (MH+).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08598159B2 |
| Source dataset | uspto-grants-2013_12 |
| ORD ID | ord-4b85603442be4e7c9f401d6da7f47bb8 |
| Source note | uspto-grants-2013_12 |