HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 631790Generated: October 31, 2026
Oxalyl chloride → (E)-4,4,5,5,5-pentafluoro-N-[2-[(4-methyl-2-pyridyl)amino]ethyl]pent-2-enamide
https://huagongshe.com/reaction/631790
Participants
| Role | Name | HCID | Charge |
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| Reactant | Oxalyl chloride | HCID 65578 | — |
| Reactant | Diisopropylethylamine | HCID 81531 | — |
| Reactant | N-(4-methylpyridin-2-yl)ethane-1,2-diamine | HCID 10034794 | — |
| Reactant | (2E)-4,4,5,5,5-Pentafluoro-2-pentenoic acid | HCID 86691160 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | (E)-4,4,5,5,5-pentafluoro-N-[2-[(4-methyl-2-pyridyl)amino]ethyl]pent-2-enamide | HCID 89832361 | — |
Reaction Steps
(E)-4,4,5,5,5-Pentafluoropent-2-enoic acid (29 mg, 0.15 mmol) was dissolved in DMF (1 ml), oxalyl chloride was added (13 μl, 0.15 mmol) and the solution was stirred at room temperature for 5 minutes. To this solution was added a solution of N′-(4-methyl-2-pyridyl)ethane-1,2-diamine (19 mg, 0.1 mmol) in DMF (0.5 ml) and diisopropylethylamine (51 μl, 0.3 mmol) and the resulting mixture was stirred at room temperature for two hours. The reaction mixture was diluted with ethyl acetate, washed with sat. sodium bicarbonate solution and brine and dried over magnesium sulfate. The volatiles were removed under reduced pressure and the residue obtained was purified by preparative HPLC (Waters XBridge, gradient of water containing 0.1% NH3 and 10% to 100% acetonitrile) to yield 18.5 mg (0.057 mmol, 57%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09321724B2 |
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| Source dataset | uspto-grants-2016_04 |
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| ORD ID | ord-8c35979386a74383b5ff2310ce289007 |
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| Source note | uspto-grants-2016_04 |
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