Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Tetrahydrofuran | HCID 8028 | — |
| Reactant | HCID 25007188 | HCID 25007188 | — |
| Reactant | HCID 178418255 | HCID 178418255 | — |
| Solvent | Water | HCID 962 | — |
| Product | HCID 66775067 | HCID 66775067 | — |
Reaction Steps
0.2 mL of a phenyl magnesium bromide 3.0 M tetrahydrofuran solution was added at 0° C. to a tetrahydrofuran (dehydrated) 3 mL solution of 200 mg of 5-(methylsulfonyl)-7-(5-(trifluoromethyl)pyridin-2-yl)-[1,2,4]triazolo[1,5-a]pyrimidine, followed by stirring at 0° C. for 5 minutes. After completion of the reaction, water was added to the reaction liquid, followed by extraction with ethyl acetate, the organic layer was dried over anhydrous sodium sulfate, and the solvent was distilled off under reduced pressure. The residue was purified by silica gel column chromatography (eluent: n-hexane/ethyl acetate=4/1) to obtain 93 mg of the desired product.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US08124760B2 |
|---|
| Source dataset | uspto-grants-2012_02 |
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| ORD ID | ord-778ccd8a6189424b8ea7417eb5655df9 |
|---|
| Source note | uspto-grants-2012_02 |
|---|