HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1926596Generated: October 26, 2026
Citric Acid → 4-[(4-methylpiperazin-1-yl)methyl]-N-{5-methyl-4-[(4-(pyrid-3-yl)pyrimid-2-yl)amino]pyrid-2-yl}-3-(trifluoromethyl)benzamide
https://huagongshe.com/reaction/1926596
Participants
| Role | Name | HCID | Charge |
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| Reactant | Citric Acid | HCID 311 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | 2-(Methylsulfonyl)-4-(pyridin-3-yl)pyrimidine | HCID 46909855 | — |
| Reactant | N-(4-amino-5-methylpyridin-2-yl)-4-[(4-methylpiperazin-1-yl)methyl]-3-(trifluoromethyl)benzamide | HCID 69229345 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Solvent | Chloroform methanol | HCID 21584188 | — |
| Product | 4-[(4-methylpiperazin-1-yl)methyl]-N-{5-methyl-4-[(4-(pyrid-3-yl)pyrimid-2-yl)amino]pyrid-2-yl}-3-(trifluoromethyl)benzamide | HCID 69231860 | — |
Reaction Steps
To a flask was added N-(4-amino-5-methylpyridin-2-yl)-4-[(4-methylpiperazin-1-yl)methyl]-3-(trifluoromethyl)benzamide (7.1 g), 2-mesyl-4-(3-pyridyl)pyrimidine (5.0 g) and DMF (50 mL). After the solution was cooled to about 0° C., sodium hydride (60%, 1.5 g) was added in several portions and the reaction was stirred at the same temperature for 2 hours, then warmed up to room temperature for 1 hour. A mixture solvent of chloroform/methanol (30:1, 100 mL) was added and the PH value was adjusted to 7 using 10% citric acid. The aqueous phase was extracted, then the organic combined phase was washed with brine, dried, filtered, concentrated and Purified through column chromatography to give the title compound.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08183242B2 |
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| Source dataset | uspto-grants-2012_05 |
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| ORD ID | ord-58a96b113ae14d62a77ed7eac51ac972 |
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| Source note | uspto-grants-2012_05 |
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