HuagongsheHuagongshe Chemistry Print Report · For research reference only
Quinoline-6-carbonyl chloride → N-(3-dimethylaminophenyl)-4-methyl-3-(6-quinolylcarbonylamino)benzamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Quinoline-6-carbonyl chloride | HCID 12391963 | — |
| Reactant | 3-amino-N-(3-dimethylaminophenyl)-4-methylbenzamide | HCID 22636111 | — |
| Product | N-(3-dimethylaminophenyl)-4-methyl-3-(6-quinolylcarbonylamino)benzamide | HCID 9802441 | — |
Reaction Steps
Using an analogous procedure to that described in Example 2, 6-quinolylcarbonyl chloride was reacted with 3-amino-N-(3-dimethylaminophenyl)-4-methylbenzamide to give the title compound; NMR Spectrum: (DMSOd6) 2.35 (s, 3H), 2.91 (s, 6H), 6.58 (m, 1H), 7.2 (m, 2H), 7.43 (d, 1H), 7.65 (m, 1H), 7.82 (d, 1H), 8.01 (s, 1H), 8.17 (m, 2H), 8.32 (d, 1H), 8.59 (d, 1H), 8.7 (d, 1H), 9.02 (s, 1H), 10.05 (s, 1H), 10.32 (s, 1H); Mass Spectrum: M+H+ 425.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06821965B1 |
| Source dataset | uspto-grants-2004_11 |
| ORD ID | ord-4dbd584a963c4d3ab6a2ade2a582de8c |
| Source note | uspto-grants-2004_11 |