HuagongsheHuagongshe Chemistry Print Report · For research reference only
Quinoline-6-carbonyl chloride → 4-methyl-N-(3-morpholinophenyl)-3-(6-quinolylcarbonylamino)benzamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Quinoline-6-carbonyl chloride | HCID 12391963 | — |
| Reactant | 3-amino-4-methyl-N-(3-morpholinophenyl)benzamide | HCID 22636145 | — |
| Product | 4-methyl-N-(3-morpholinophenyl)-3-(6-quinolylcarbonylamino)benzamide | HCID 22636159 | — |
Reaction Steps
Using an analogous procedure to that described in Example 1, 6-quinolylcarbonyl chloride was reacted with 3-amino-4-methyl-N-(3-morpholinophenyl)benzamide to give the title compound; NMR Spectrum: (DMSOd6) 2.35 (s, 3H), 3.0-3.1 (m, 4H), 3.65-3.75 (m, 4H), 6.65-6.7 (m, 1H), 7.17 (t, 1H), 7.3-7.35 (m, 1H), 7.38-7.48 (m, 2H), 7.6-7.7 (m, 1H), 7.8-7.85 (m, 1H), 8.0 (s, 1H), 8.1-8.15 (m, 1H), 8.3-8.35 (m, 1H), 8.5-8.55 (m, 1H), 8.7 (s, 1H), 8.98-9.02 (m, 1H), 10.0-10.1 (br s, 1H), 10.25-10.35 (br s, 1H); Mass Spectrum: M+H+ 467.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06821965B1 |
| Source dataset | uspto-grants-2004_11 |
| ORD ID | ord-5baacfec9bc24301994773a051051e87 |
| Source note | uspto-grants-2004_11 |