HuagongsheHuagongshe Chemistry Print Report · For research reference only
Triethylamine → 2-(Pivaloylamino)pyridine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | 2-Aminopyridine | HCID 10439 | — |
| Reactant | Pivaloyl chloride | HCID 62493 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 2-(Pivaloylamino)pyridine | HCID 1051519 | — |
Reaction Steps
1.1 equivalents of pivalic acid chloride dissolved in 100 ml of dichloromethane are added dropwise at 0° C. to a solution containing one equivalent of 2-aminopyridine and 1.25 equivalents of triethylamine in 400 ml of dichloromethane. Once the addition is complete, the reaction mixture is brought to room temperature for three hours, and then the reaction mixture is washed with a saturated NaHCO3 solution. After drying of the organic phase, filtration and concentration under reduced pressure, the resulting residue is crystallised from hexane, enabling the expected product to be isolated by filtration.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06127369 |
| Source dataset | uspto-grants-2000_10 |
| ORD ID | ord-fbe15bd0863943bc870ad837900d4d26 |
| Source note | uspto-grants-2000_10 |