Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Sodium Iodide | HCID 5238 | — |
| Reactant | Chlorotrimethylsilane | HCID 6397 | — |
| Reactant | HCID 117988134 | HCID 117988134 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | HCID 117988005 | HCID 117988005 | 92.8% |
Reaction Steps
To a solution of 4-(3-cyclopentyl-7-methoxy-1H-pyrazolo[3,4-c]pyridin-1-yl)benzenesulfonamide (22.4 mg) in acetonitrile (10 mL) were added sodium iodide (18.0 mg) and chloro(trimethyl)silane (52.1 mg), and the mixture was stirred at 80° C. for 5 hr. To the reaction mixture was added water at room temperature, and the mixture was extracted with ethyl acetate. The organic layer was washed with water and saturated brine, dried over anhydrous magnesium sulfate, and concentrated under reduced pressure. The residue was purified by silica gel column chromatography (ethyl acetate/hexane) to give the title compound (20 mg).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09371320B2 |
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| Source dataset | uspto-grants-2016_06 |
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| ORD ID | ord-4275afc9215b4d6b8fc80112189f5b01 |
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| Source note | uspto-grants-2016_06 |
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