HuagongsheHuagongshe Chemistry Print Report · For research reference only
Thionyl Chloride → HCID 86303959, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Thionyl Chloride | HCID 24386 | — |
| Reactant | HCID 86303956 | HCID 86303956 | — |
| Reactant | HCID 90415043 | HCID 90415043 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 86303959 | HCID 86303959 | — |
Reaction Steps
5-(Chloro(4-fluorophenyl)methyl)-3-(3-chlorophenyl)-2-methoxypyridine. To a cooled solution, 0° C., of [5-(3-chlorophenyl)-6-methoxypyridin-3-yl](4-fluorophenyl)methanol (Example 14, 1.43 g, 4.17 mmol), in DCM (10 mL), was added thionyl chloride (744 mg, 6.25 mmol) dropwise. The solution was allowed to warm up to room temperature, and stirred for 1 h. The reaction mixture was concentrated under reduced pressure. Purification (FCC, SiO2, 0-10% EtOAc/hexanes) afforded the title compound, which was used directly for the next step.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09120770B2 |
| Source dataset | uspto-grants-2015_09 |
| ORD ID | ord-ec8733f530304afeaa0001253c283d1c |
| Source note | uspto-grants-2015_09 |