HuagongsheHuagongshe Chemistry Print Report · For research reference only
Oxalyl chloride → (E)-4,4,4-Trifluoro-N-[2-[(6-methoxy-2-methyl-3-pyridyl)amino]ethyl]but-2-enamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Oxalyl chloride | HCID 65578 | — |
| Reactant | Diisopropylethylamine | HCID 81531 | — |
| Reactant | 4,4,4-Trifluorocrotonic acid | HCID 5709614 | — |
| Reactant | N-(6-Methoxy-2-methyl-3-pyridyl)ethane-1,2-diamine | HCID 89825702 | — |
| Catalyst | Dichloromethane | HCID 6344 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | (E)-4,4,4-Trifluoro-N-[2-[(6-methoxy-2-methyl-3-pyridyl)amino]ethyl]but-2-enamide | HCID 71811866 | 23.3% |
Reaction Steps
(E)-4,4,4-Trifluorobut-2-enoic acid (33 mg, 0.23 mmol) was dissolved in DCM (1 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-(6-methoxy-2-methyl-3-pyridyl)ethane-1,2-diamine (27 mg, 0.15 mmol) and diisopropylethylamine (88 μl, 0.5 mmol) 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 (Waters XBridge, gradient of water containing 0.1% NH3 and 10% to 100% acetonitrile) to yield 10.5 mg of a solid (0.035 mmol, 23%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09321724B2 |
| Source dataset | uspto-grants-2016_04 |
| ORD ID | ord-8f9d2edbdc42438ca278d293e455a272 |
| Source note | uspto-grants-2016_04 |