HuagongsheHuagongshe Chemistry Print Report · For research reference only
4-Chloroaniline → N-(4-chlorophenyl)-6-(6,7-dimethoxyquinolin-4-yloxy)benzofuran-3-carboxamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 4-Chloroaniline | HCID 7812 | — |
| Reactant | Diisopropylethylamine | HCID 81531 | — |
| Reactant | O-(Benzotriazol-1-yl)-N,N,N',N'-tetramethyluronium tetrafluoroborate | HCID 2733207 | — |
| Reactant | 6-(6,7-Dimethoxyquinolin-4-yloxy)benzofuran-3-carboxylic acid | HCID 69018682 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | N-(4-chlorophenyl)-6-(6,7-dimethoxyquinolin-4-yloxy)benzofuran-3-carboxamide | HCID 57975990 | 12.4% |
Reaction Steps
6-(6,7-Dimethoxyquinolin-4-yloxy)benzofuran-3-carboxylic acid (31 mg, 0.085 mmol) and 2-(1H-benzotriazole-1-yl)-1,1,3,3-tetramethyluronium tetrafluoroborate (41 mg, 0.127 mmol) were added to a reaction tube then dissolved in DMF (0.6 mL). 4-chloroaniline (13 mg, 0.102 mmol) was added to the reaction mixture, followed by N,N-diisopropylethylamine (22 mg, 0.17 mmol) and stirring was continued for 2 days. The mixture was concentrated in vacuo. The remaining orange oil was purified by silica gel chromatography (1% to 2% methanol in dichloromethane) to afford N-(4-chlorophenyl)-6-(6,7-dimethoxyquinolin-4-yloxy)benzofuran-3-carboxamide as a yellow solid (5 mg). MS (ESI, pos. ion) m/z: 475.1 (M+1). Mass calc'd for C26H19ClN2O5: 474.89.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07626030B2 |
| Source dataset | uspto-grants-2009_12 |
| ORD ID | ord-601e30b1dbef4c9f93f52ca5b518f8be |
| Source note | uspto-grants-2009_12 |