HuagongsheHuagongshe Chemistry Print Report · For research reference only
6-Quinolinecarboxylic acid → N-[5-(3-cyclohexylpropionamido)-2-methylphenyl]quinoline-6-carboxamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 6-Quinolinecarboxylic acid | HCID 82571 | — |
| Reactant | N-(3-amino-4-methylphenyl)-3-cyclohexylpropionamide | HCID 10777768 | — |
| Product | N-[5-(3-cyclohexylpropionamido)-2-methylphenyl]quinoline-6-carboxamide | HCID 22058006 | — |
Reaction Steps
Using an analogous procedure to that described in Example 5, quinoline-6-carboxylic acid was reacted with N-(3-amino-4-methylphenyl)-3-cyclohexylpropionamide to give the title compound; NMR Spectrum: (DMSOd6) 0.76-1.28 (m, 6H), 1.42-1.78 (m, 7H), 2.2 (s, 3H), 2.28 (t, 2H), 7.17 (d, 1H), 7.39 (d, 1H), 7.6 (m, 1H)), 7.69 (s, 1H), 8.12 (d, 1H), 8.24 (d, 1H), 8.49 (d, 1H), 8.63 (s, 1H), 9.0 (m, 1H), 9.82 (s, 1H), 10.09 (s, 1H); Mass Spectrum: M+H+ 437.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06432949B1 |
| Source dataset | uspto-grants-2002_08 |
| ORD ID | ord-ddfc97a9ca9e431d807a99ccc2a039d6 |
| Source note | uspto-grants-2002_08 |