HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 631796Generated: October 31, 2026
Oxalyl chloride → (E)-N-[2-[(4-Ethoxy-2-pyridyl)amino]ethyl]-4,4-difluoro-pent-2-enamide
https://huagongshe.com/reaction/631796
Participants
| Role | Name | HCID | Charge |
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| Reactant | Oxalyl chloride | HCID 65578 | — |
| Reactant | Diisopropylethylamine | HCID 81531 | — |
| Reactant | (E)-4,4-Difluoropent-2-enoic acid | HCID 75530053 | — |
| Reactant | N-(4-Ethoxy-2-pyridyl)ethane-1,2-diamine | HCID 89825952 | — |
| Catalyst | Dichloromethane | HCID 6344 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | (E)-N-[2-[(4-Ethoxy-2-pyridyl)amino]ethyl]-4,4-difluoro-pent-2-enamide | HCID 89832427 | 41.7% |
Reaction Steps
(E)-4,4-Difluoropent-2-enoic acid (31 mg, 0.23 mmol) was dissolved in dichloromethane (0.5 ml containing one drop of dimethyl formamide), oxalyl chloride was added (20 μl, 0.23 mmol) and the solution was stirred at room temperature for 15 minutes. This solution was added to a solution of N-(4-ethoxy-2-pyridyl)ethane-1,2-diamine (27 mg, 0.15 mmol) and diisopropylethylamine (88 μl, 0.5 mmol) dissolved in DCM (2 ml) and the resulting mixture was stirred at room temperature for three hours. The volatiles were removed under reduced pressure and the residue was purified by preparative HPLC (gradient of water containing 0.1% NH3 and 10% to 100% acetonitrile) to yield 18.7 mg of a residue that was purified again by preparative HPLC (gradient of water containing 0.1% trifluoroacetic acid and 10% to 100% acetonitrile). The product obtained was converted to the free base by dissolving in DCM, washing with 1N NaOH solution, water and evaporation to dryness under reduced pressure to yield 13.2 mg of a solid (0.044 mmol, 29%).
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-e572b33baf8849f095fc1faea1226258 |
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| Source note | uspto-grants-2016_04 |
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