HuagongsheHuagongshe Chemistry Print Report · For research reference only
6-Quinolinecarboxylic acid → HCID 9867182, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 6-Quinolinecarboxylic acid | HCID 82571 | — |
| Reactant | HCID 16793499 | HCID 16793499 | — |
| Product | HCID 9867182 | HCID 9867182 | 18% |
Reaction Steps
Using an analogous procedure to that described in Example 3, quinoline-6-carboxylic acid was reacted with N-(3-amino-4-chlorophenyl)-4-cyanobenzamide. The crude reaction product was purified by column chromatography on silica using a 97:3 mixture of methylene chloride and methanol as eluent. There was thus obtained the title compound in 18% yield; NMR Spectrum: (DMSOd6) 7.58 (d, 1H), 7.62 (m, 1H), 7.77 (m, 1H), 8.01 (d, 2H), 8.12 (t, 4H), 8.28 (d, 2H), 8.56 (d, 1H), 8.67 (s, 1H), 9.01 (d, 1H), 10.34 (s, 1H), 10.67 (s, 1H); Mass Spectrum: M−H− 425.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06432949B1 |
| Source dataset | uspto-grants-2002_08 |
| ORD ID | ord-57854f18c84c4cd38e705f744149f2e2 |
| Source note | uspto-grants-2002_08 |