HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 595309Generated: October 29, 2026
Sodium Carbonate → 1-(4-(3-((4-(difluoromethyl)pyrimidin-2-yl)amino)-5-methylphenyl)-1H-pyrazol-1-yl)propan-2-one
https://huagongshe.com/reaction/595309
Participants
| Role | Name | HCID | Charge |
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| Reactant | Sodium Carbonate | HCID 10340 | — |
| Reactant | 1-(4-bromo-1H-pyrazol-1-yl)propan-2-one | HCID 19576908 | — |
| Reactant | 4-(difluoromethyl)-N-(3-methyl-5-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl)pyrimidin-2-amine | HCID 58456171 | — |
| Catalyst | HCID 178418807 | HCID 178418807 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | 1,4-Dioxane | HCID 31275 | — |
| Product | 1-(4-(3-((4-(difluoromethyl)pyrimidin-2-yl)amino)-5-methylphenyl)-1H-pyrazol-1-yl)propan-2-one | HCID 118208798 | — |
Reaction Steps
4-(Difluoromethyl)-N-(3-methyl-5-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl)pyrimidin-2-amine (400 mg, 1.11 mmol) and 1-(4-bromo-1H-pyrazol-1-yl)propan-2-one (225 mg, 1.11 mmol) were dissolved in dioxane (4 mL) and degassed with nitrogen for 5 minutes. PdCl2(dppf)-CH2Cl2 (90 mg, 0.11 mmol) and sodium carbonate (2.0 M in water, 1.107 ml, 2.215 mmol) were added, the reaction was sealed and heated to 90° C. for 12 hours. The reaction was cooled to ambient temperature, diluted with water (10 mL) and product extracted with ethyl acetate (2×20 mL). The extracts were dried over anhydrous magnesium sulfate, filtered, and concentrated under reduced pressure to afford the crude product residue. The crude product residue was purified by column chromatography on silica (5-50% ethyl acetate/hexanes) to afford 1-(4-(3-((4-(difluoromethyl)pyrimidin-2-yl)amino)-5-methylphenyl)-1H-pyrazol-1-yl)propan-2-one. MS ESI calcd. for C18H18F2N5O [M+H]+ 358. found 358.
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-fb67d5e30c164400b63a008bae3995bc |
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| Source note | uspto-grants-2016_01 |
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