HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2199563Generated: October 29, 2026
Potassium Carbonate → 4-Methyl-2-[3-(1-methyl-piperidin-4-yl)-propylamino]-pyrimidine-5-carbonitrile
https://huagongshe.com/reaction/2199563
Participants
| Role | Name | HCID | Charge |
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| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | HCID 59154395 | HCID 59154395 | — |
| Reactant | HCID 178480300 | HCID 178480300 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | 4-Methyl-2-[3-(1-methyl-piperidin-4-yl)-propylamino]-pyrimidine-5-carbonitrile | HCID 44545777 | — |
Reaction Steps
To a 5-L round-bottom flask equipped with overhead mechanical stirrer, nitrogen inlet, and thermocouple probe were added 2-acetyl-3-dimethylamino -acrylonitrile (103.65 g, 0.75 mol), anhydrous potassium carbonate (powdered, not granular) (165.85 g, 1.2 mol), and N-[3-(1-methyl-piperidin-4-yl)-propyl]-guanidine (119.02 g, 0.60 mol) in ethanol (2.125 L). The resultant mixture was heated to reflux with stirring and held for 24 h. The resultant mixture was then concentration and the resultant residue partitioned between ethyl acetate (1.5 L) and 1 N NaOH (1.5 L). The layers were separated and the aqueous layer was extracted with additional ethyl acetate (2×1.5 L). The combined organic layers were concentrated to yield the title compound as a solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09359327B2 |
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| Source dataset | uspto-grants-2016_06 |
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| ORD ID | ord-918fb66c07664636ad95626204f40dd5 |
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| Source note | uspto-grants-2016_06 |
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