HuagongsheHuagongshe Chemistry Print Report · For research reference only
Dimethylformamide → 3,5-difluoro-4-methoxy-N-[4-(6-methylimidazo[1,2-a]pyridin-2-yl)phenyl]benzamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Dimethylformamide | HCID 6228 | — |
| Reactant | 4-(6-Methylimidazo[1,2-a]pyridin-2-yl)aniline | HCID 821084 | — |
| Reactant | 3,5-Difluoro-4-methoxybenzoic acid | HCID 2736987 | — |
| Reactant | Dichloromethane methanol | HCID 21226129 | — |
| Solvent | Pyridine | HCID 1049 | — |
| Solvent | Thionyl Chloride | HCID 24386 | — |
| Product | 3,5-difluoro-4-methoxy-N-[4-(6-methylimidazo[1,2-a]pyridin-2-yl)phenyl]benzamide | HCID 58342121 | 62.6% |
Reaction Steps
To a stirred solution of 3,5-difluoro-4-methoxybenzoic acid (0.25 g, 1.34 mmol) in thionyl chloride (4 ml) was added a drop of DMF and the reaction mixture was then heated under reflux for 5 h. On cooling to room temperature the excess reagent was removed under reduced pressure to give a crude residue. The amide was prepared as described in the Amide Coupling section using the crude residue and 4-(6-methylimidazo[1,2-a]pyridin-2-yl)aniline (0.30 g, 1.34 mmol) in dry pyridine (14 ml) to give the title compound (0.33 g, 62%) as a pale yellow solid after work-up and flash chromatography (DCM/MeOH 20:1).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08895313B2 |
| Source dataset | uspto-grants-2014_11 |
| ORD ID | ord-c05859eebf82498388ff812ae4f7885f |
| Source note | uspto-grants-2014_11 |