HuagongsheHuagongshe Chemistry Print Report · For research reference only
Oxalyl chloride → N-methyl-4-[4-[(E)-4,4,5,5-tetrafluoropent-2-enoyl]piperazin-1-yl]pyridine-2-carboxamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Oxalyl chloride | HCID 65578 | — |
| Reactant | Diisopropylethylamine | HCID 81531 | — |
| Reactant | N-Methyl-4-piperazin-1-yl-pyridine-2-carboxamide hydrochloride | HCID 66835948 | — |
| Reactant | (E)-4,4,5,5-tetrafluoropent-2-enoic acid | HCID 86691165 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | N-methyl-4-[4-[(E)-4,4,5,5-tetrafluoropent-2-enoyl]piperazin-1-yl]pyridine-2-carboxamide | HCID 56949207 | — |
Reaction Steps
(E)-4,4,5,5-tetrafluoropent-2-enoic acid (19 mg, 0.11 mmol) was dissolved in DCM (1 ml), oxalyl chloride was added (9 μl, 0.11 mmol) followed by a drop of DMF. The mixture was stirred for 10 minutes at room temperature. N-methyl-4-piperazin-1-yl-pyridine-2-carboxamide hydrochloride (25.6 mg, 0.1 mmol) was dissolved in DMF (0.5 ml), the mixtures were combined, diisopropylethylamine (75 μl, 0.4 mmol) was added and the resulting mixture was stirred at room temperature for 1 hour. The mixture was evaporated to dryness under reduced pressure, the residue was purified by preparative HPLC (gradient of water containing 0.1% NH3 and acetonitrile) to yield 20.2 mg (0.054 mmol, 54%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08883791B2 |
| Source dataset | uspto-grants-2014_11 |
| ORD ID | ord-13210a72890846eb8d8fe909b79d9e75 |
| Source note | uspto-grants-2014_11 |