HuagongsheHuagongshe Chemistry Print Report · For research reference only
Oxalyl chloride → (E)-4,4-Difluoro-1-[(3R)-3-[(4-methyl-2-pyridyl)amino]-1-piperidyl]pent-2-en-1-one
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Oxalyl chloride | HCID 65578 | — |
| Reactant | Diisopropylethylamine | HCID 81531 | — |
| Reactant | (E)-4,4-Difluoropent-2-enoic acid | HCID 75530053 | — |
| Reactant | 4-Methyl-N-[(3R)-3-piperidyl]pyridin-2-amine dihydrochloride | HCID 89825961 | — |
| Catalyst | Dimethylformamide | HCID 6228 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | (E)-4,4-Difluoro-1-[(3R)-3-[(4-methyl-2-pyridyl)amino]-1-piperidyl]pent-2-en-1-one | HCID 117951678 | 48.3% |
Reaction Steps
(E)-4,4-Difluoropent-2-enoic acid (22 mg, 0.16 mmol) was dissolved in dichloromethane (1 ml), oxalyl chloride (14 μl, 0.16 mol) and one drop of DMF were added and the resulting solution was stirred at room temperature for 15 minutes. This solution was added to a solution of 4-methyl-N-[(3R)-3-piperidyl]pyridin-2-amine dihydrochloride (23 mg, 0.087 mmol) in DCM (2 ml). Ethyl-N,N-diisopropylamine (DIPEA, 70 μl, 0.4 mmol) was added and the resulting mixture was stirred at room temperature overnight. The mixture was concentrated under reduced pressure and the resulting residue was purified by preparative HPLC (Waters X-bridge, gradient of water containing 0.1% NH3 and acetonitrile) to yield 13 mg of a solid (0.042 mmol, 48%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09260441B2 |
| Source dataset | uspto-grants-2016_02 |
| ORD ID | ord-421c27647cb3436f9b107ee38d8f635e |
| Source note | uspto-grants-2016_02 |