HuagongsheHuagongshe Chemistry Print Report · For research reference only
Piperidin-4-ol → HCID 71217368, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Piperidin-4-ol | HCID 79341 | — |
| Reactant | HCID 71208954 | HCID 71208954 | — |
| Product | HCID 71217368 | HCID 71217368 | — |
Reaction Steps
2-(4-Hydroxypiperidin-1-yl)-thiazole-5-carboxylic acid (7-chloro-4-oxo-1-phenyl-1,4-dihydro-quinolin-3-ylmethyl)-amide was prepared starting from intermediate F and 4-hydroxypiperidine. 1H NMR (400 MHz, DMSO-d6) δ ppm 8.48 (t, J=5.54 Hz, 1H) 8.25 (d, J=8.66 Hz, 1H) 7.91 (s, 1H) 7.78 (s, 1H) 7.59-7.71 (m, 3H) 7.54-7.59 (m, 1H) 7.43 (dd, J=8.66, 2.01 Hz, 1H) 6.88 (d, J=1.81 Hz, 1H) 4.79 (d, J=4.03 Hz, 1H) 4.26 (d, J=5.44 Hz, 2H) 3.69 (dd, J=12.59, 4.53 Hz, 3H) 3.20 (ddd, J=13.09, 9.37, 3.53 Hz, 2H) 1.70-1.81 (m, 2H) 1.39 (td, J=8.66, 4.23 Hz, 2H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08501732B2 |
| Source dataset | uspto-grants-2013_08 |
| ORD ID | ord-a2ff7d9686494c47a202813953c56403 |
| Source note | uspto-grants-2013_08 |