HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1428115Generated: October 31, 2026
Cesium carbonate → 3-(4-Aminophenyl)-5-{1-[(2S)-1,4-dioxan-2-ylmethyl]-1H-pyrazol-4-yl}pyridin-2-amine
https://huagongshe.com/reaction/1428115
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Cesium carbonate | HCID 10796 | — |
| Reactant | 4-(4,4,5,5-Tetramethyl-1,3,2-dioxaborolan-2-yl)-1H-pyrazole | HCID 2774010 | — |
| Reactant | 3-(4-Aminophenyl)-5-bromopyridin-2-amine | HCID 68288976 | — |
| Reactant | (2R)-1,4-dioxan-2-ylmethyl methanesulfonate | HCID 86609782 | — |
| Catalyst | Tetrabutylammonium Iodide | HCID 67553 | — |
| Catalyst | HCID 178418807 | HCID 178418807 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Solvent | 1,4-Dioxane | HCID 31275 | — |
| Product | 3-(4-Aminophenyl)-5-{1-[(2S)-1,4-dioxan-2-ylmethyl]-1H-pyrazol-4-yl}pyridin-2-amine | HCID 86700068 | 71% |
Reaction Steps
4-(4,4,5,5-Tetramethyl-1,3,2-dioxaborolan-2-yl)-1H-pyrazole (10.0 g) was added to a suspension of cesium carbonate (75.6 g) in 1,4-dioxane (200 ml), followed by stirring. (2R)-1,4-Dioxan-2-ylmethyl methanesulfonate (12.1 g) and tetra-n-butylammonium iodide (0.95 g) were then added, and the mixture was stirred at 100° C. for six hours. After cooling the reaction solution to room temperature, 3-(4-aminophenyl)-5-bromopyridin-2-amine (10.9 g) and [1,1′-bis(diphenylphosphino)ferrocene]palladium(II) dichloride-dichloromethane adduct (2.1 g) were added, and the mixture was stirred at 100° C. for one hour. The reaction solution was returned to room temperature, ethyl acetate was added, and the insoluble matter was then removed by filtration. The resulting organic layer was sequentially washed with water and brine and then dried over anhydrous sodium sulfate. The solvent was distilled off under reduced pressure, and the residue was purified by silica gel column chromatography [chloroform:methanol=99:1->19:1 (v/v)] to give 10.3 g of the title compound as a solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08933103B2 |
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| Source dataset | uspto-grants-2015_01 |
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| ORD ID | ord-69a61730e452476bb4d37b20566c34e4 |
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| Source note | uspto-grants-2015_01 |
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