HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 595311Generated: October 31, 2026
Cesium carbonate → 4-(1-fluoroethyl)-N-(3-methyl-5-(1-(2-methylallyl)-1H-pyrazol-4-yl)phenyl)pyrimidin-2-amine
https://huagongshe.com/reaction/595311
Participants
| Role | Name | HCID | Charge |
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| Reactant | Cesium carbonate | HCID 10796 | — |
| Reactant | 1,1'-(9,9-Dimethyl-9H-xanthene-4,5-diyl)bis(1,1-diphenylphosphine) | HCID 636044 | — |
| Reactant | 2-Chloro-4-(1-fluoroethyl)pyrimidine | HCID 86658237 | — |
| Reactant | 3-methyl-5-(1-(2-methylallyl)-1H-pyrazol-4-yl)aniline | HCID 118208642 | — |
| Catalyst | palladium(II) acetate | HCID 167845 | — |
| Solvent | 1,4-Dioxane | HCID 31275 | — |
| Product | 4-(1-fluoroethyl)-N-(3-methyl-5-(1-(2-methylallyl)-1H-pyrazol-4-yl)phenyl)pyrimidin-2-amine | HCID 118208622 | — |
Reaction Steps
2-Chloro-4-(1-fluoroethyl)pyrimidine (170 mg, 1.06 mmol), Palladium(II) acetate (59.3 mg, 0.26 mmol), 4,5-bis(diphenylphosphino)-9,9-dimethylxanthene (229 mg, 0.40 mmol), and cesium carbonate (860 mg, 2.64 mmol) were added to a solution of 3-methyl-5-(1-(2-methylallyl)-1H-pyrazol-4-yl)aniline (300 mg, 1.32 mmol) in dioxane (2.5 mL). The solution was degassed by sparging with Ar for 5 minutes and stirred at 110° C. for 18 h. The mixture was allowed to cool to room temperature, diluted with EtOAc, and washed with brine. The organic layer was dried over anhydrous magnesium sulfate, filtered and concentrated under reduced pressure. The residue was purified by column chromatography on silica gel (10-30% EtOAc/Hexane), then further purified by reverse phase HPLC (ACN/water with 0.1% TFA modifier) to afford 4-(1-fluoroethyl)-N-(3-methyl-5-(1-(2-methylallyl)-1H-pyrazol-4-yl)phenyl)pyrimidin-2-amine MS ESI calc'd. for C20H23FN5 [M+H]+ 352. found 352.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09242984B2 |
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| Source dataset | uspto-grants-2016_01 |
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| ORD ID | ord-5a65205af67d4972abb1685dc6e1b1c4 |
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| Source note | uspto-grants-2016_01 |
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