HuagongsheHuagongshe Chemistry Print Report · For research reference only
Pyridine → HCID 16743933, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Pyridine | HCID 1049 | — |
| Reactant | (-)-alpha-Methoxy-alpha-(trifluoromethyl)phenylacetyl chloride | HCID 3080792 | — |
| Reactant | 1-(5-Chloropyridin-2-yl)-1-(3-fluoro-5-(trifluoromethyl)phenyl)-2-phenylethanamine | HCID 59134573 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 16743933 | HCID 16743933 | — |
Reaction Steps
To racemic 1-(5-chloropyridin-2-yl)-1-(3-fluoro-5-(trifluoromethyl)phenyl)-2-phenylethanamine (obtained as described in Example 1, Procedure 1) (55 mg, 0.14 mmol) in DCM (1 mL) was added pyridine (56 μL, 55 mmol) and (R)-3,3,3-trifluoro-2-methoxy-2-phenylpropanoyl chloride (52 μL, 0.22 mmol). The reaction was stirred at room temperature for 14 h and the reaction mixture filtered through a silica plug elution with DCM. (S)-N-((S)-1-(5-chloropyridin-2-yl)-1-(3-fluoro-5-(trifluoromethyl)phenyl)-2-phenylethyl)-3,3,3-trifluoro-2-methoxy-2-phenylpropanamide was crystallized from ether heptane.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07652023B2 |
| Source dataset | uspto-grants-2010_01 |
| ORD ID | ord-0c2dbe612c894819924ff6aefb9248d4 |
| Source note | uspto-grants-2010_01 |