HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 220078Generated: October 25, 2026
Cesium carbonate → N-{4-Methyl-3-[2-methyl-4-(6-methylsulfanyl-pyrimidin-4-yl)-2H-pyrazol-3-ylamino]-phenyl}-3-trifluoromethyl-benzamide
https://huagongshe.com/reaction/220078
Participants
| Role | Name | HCID | Charge |
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| Reactant | Cesium carbonate | HCID 10796 | — |
| Reactant | 1,4-Dioxane | HCID 31275 | — |
| Reactant | N-(3-Bromo-4-Methylphenyl)-3-(Trifluoromethyl)Benzamide | HCID 58601069 | — |
| Reactant | 2-Methyl-4-(6-methylsulfanyl-pyrimidin-4-yl)-2H-pyrazol-3-ylamine | HCID 59173302 | — |
| Catalyst | palladium(II) acetate | HCID 167845 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | N-{4-Methyl-3-[2-methyl-4-(6-methylsulfanyl-pyrimidin-4-yl)-2H-pyrazol-3-ylamino]-phenyl}-3-trifluoromethyl-benzamide | HCID 59173636 | — |
Reaction Steps
2-Methyl-4-(6-methylsulfanyl-pyrimidin-4-yl)-2H-pyrazol-3-ylamine (120 mg, 0.54 mmol) is mixed with N-(3-Bromo-4-methyl-phenyl)-3-trifluoromethyl-benzamide (290 mg, 0.81 mmol), palladium acetate (25 mg, 0.1 mmol), Xantophos (100 mg, 0.17 mmol) and cesium carbonate (530 mg, 1.63 mmol). 10 mL of anhydrous 1,4-dioxane is added under a nitrogen environment and the mixture is subjected to microwave irradiation to 150° C. for one hour. The reaction mixture is then cooled to room temperature, treated with 100 mL THF, passed through a celite column and concentrated. The crude product is purified by ISCO chromatography eluting with ethyl acetate in hexanes from 10% to 100% to afford N-{4-Methyl-3-[2-methyl-4-(6-methylsulfanyl-pyrimidin-4-yl)-2H-pyrazol-3-ylamino]-phenyl}-3-trifluoromethyl-benzamide: MS m/z 499.1 (M+1).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08202876B2 |
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| Source dataset | uspto-grants-2012_06 |
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| ORD ID | ord-e666274769674ed785f5d9ad4ef36895 |
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| Source note | uspto-grants-2012_06 |
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