Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Cesium carbonate | HCID 10796 | — |
| Reactant | HCID 86657920 | HCID 86657920 | — |
| Reactant | HCID 178477882 | HCID 178477882 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | HCID 86657919 | HCID 86657919 | 88% |
Reaction Steps
To a solution of 2-chloro-4-[3-(5-chloro-2-thienyl)-1H-pyrazol-4-yl]pyridine (6.7 mmol) in 53 mL N,N-dimethylformamide were added bromoisobutyle (10.1 mmol) and cesium carbonate (7.4 mmol). The reaction mixture was stirred overnight at room temperature and the solvent was then evaporated. The residue was diluted with water and extracted three times with ethyl acetate. The combined organic extracts were dried over MgSO4, filtered and concentrated. The residue was purified by chromatography on silica gel (heptane:ethyl acetate 1:0 to 1:1) to afford 2.21 g of a mixture of 2-chloro-4-[1-isobutyl-3-(5-chloro-2-thienyl)-1H-pyrazol-4-yl]pyridine and 2-chloro-4-[1-isobutyl-5-(5-chloro-2-thienyl)-1H-pyrazol-4-yl]pyridine (8:2; 88% yield). The mixture was used as such in the next step.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08685974B2 |
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| Source dataset | uspto-grants-2014_04 |
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| ORD ID | ord-f5e5c72885034f7fa0c89731d5ae021b |
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| Source note | uspto-grants-2014_04 |
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