HuagongsheHuagongshe Chemistry Print Report · For research reference only
Triethylamine → HCID 22027358, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | HCID 22027357 | HCID 22027357 | — |
| Reactant | 2,4-Dichloropyridine-3-carbonyl chloride | HCID 22027362 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 22027358 | HCID 22027358 | — |
Reaction Steps
2,4-Dichloronicotinoyl chloride (0.40 g), made as in Example 1, Step C, was added to a solution of the amine intermediate from Step A (0.66 g) and triethylamine (0.70 g) in 30 mL of methylene chloride at room temperature followed by stirring overnight. The reaction mixture was distilled under vacuum to remove the solvent, giving an oil that was filtered through silica gel using 100% methylene chloride as the eluent. The solvent was then removed under vacuum to give the title compound, a compound of the invention, as a red oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07074742B2 |
| Source dataset | uspto-grants-2006_07 |
| ORD ID | ord-b92e03430ce64cfd8549db8cb98d780c |
| Source note | uspto-grants-2006_07 |