Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Thionyl Chloride | HCID 24386 | — |
| Reactant | HCID 57799417 | HCID 57799417 | — |
| Solvent | 1,2-Dichloroethane | HCID 11 | — |
| Product | HCID 57799456 | HCID 57799456 | — |
Reaction Steps
To a stirring solution of 3-((7-(4-chlorophenyl)-3-oxo-8-(pyridin-4-yl)-[1,2,4]triazolo[4,3-a]pyridin-2(3H)-yl)methyl)-6-(trifluoromethyl)picolinic acid (71 mg, 0.133 mmol) in anhydrous ClCH2CH2Cl (1 mL) at room temperature was added dropwise thionyl chloride (2 mL). The mixture was then stirred at 80° C. for 1 h. After cooling to room temperature, the reaction mixture was concentrated under reduced pressure. The residue was evaporated with toluene (5 mL×2), and dried in high vacuum to afford the title compound (72 mg) as a yellow foam, which was used in the next reaction without further purification.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US07572808B2 |
|---|
| Source dataset | uspto-grants-2009_08 |
|---|
| ORD ID | ord-efbaa33dc43444c08d3c0875891456b2 |
|---|
| Source note | uspto-grants-2009_08 |
|---|