HuagongsheHuagongshe Chemistry Print Report · For research reference only
Piperidine → HCID 22057989, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Piperidine | HCID 8082 | — |
| Reactant | HCID 22058010 | HCID 22058010 | — |
| Product | HCID 22057989 | HCID 22057989 | 96% |
Reaction Steps
Using an analogous procedure to that described in Example 21, N-[2-chloro-5-(2-chloropyrid-4-ylcarbonylamino)phenyl]-2-chloropyridine-4-carboxamide was reacted with piperidine to give the title compound in 96% yield; NMR Spectrum: (DMSOd6) 1.6 (m, 12H), 3.58 (m, 8H), 7.01 (m, 2H), 7.24 (d, 2H), 7.54 (d, 1H), 7.73 (d, 1H), (m, 2H), 10.09 (br s, 1H), 10.44 (br s, 1H); Mass Spectrum: M+H+ 519.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06432949B1 |
| Source dataset | uspto-grants-2002_08 |
| ORD ID | ord-ba2755717d0742798e0f1bec4e34d01a |
| Source note | uspto-grants-2002_08 |