HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ethyl 4-oxo-1-piperidinecarboxylate → HCID 136365333, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ethyl 4-oxo-1-piperidinecarboxylate | HCID 34767 | — |
| Reactant | HCID 136365334 | HCID 136365334 | — |
| Product | HCID 136365333 | HCID 136365333 | — |
Reaction Steps
This was prepared by the method of Example 173 using 2-hydroxy-6-aminobenzamidine dihydrochloride (Example D) and ethyl 4-oxopiperidine-1-carboxylate to give the title compound as a yellow solid, MS (+CI) 305 ([M+H]+), 1H NMR (d6 -DMSO) 11.80 (1H, s), 9.96 (1H, s), 8.64 (1H, s), 8.54 (1H, s), 7.49 (1H, s), 7.23 (1H, t), 6.31 (1H, d), 6.27 (1H, d), 4.02-4.08 (2H, m), 3.5-3.7 (2H, m), 3.3-3.5 (2H, m), 1.6-1.8 (2H, m), 1.19 (3H, t).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05883102 |
| Source dataset | uspto-grants-1999_03 |
| ORD ID | ord-083b7ddf29e94f65b1c562eb759b2622 |
| Source note | uspto-grants-1999_03 |