HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 236678Generated: October 25, 2026
Potassium Carbonate → N,N-Diethyl-6-methyl-2-(4-pyridinyl)-4-pyrimidinamine
https://huagongshe.com/reaction/236678
Participants
| Role | Name | HCID | Charge |
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| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | Diethylammonium chloride | HCID 10197650 | — |
| Reactant | 4-Chloro-6-methyl-2-(pyridin-4-yl)pyrimidine | HCID 12764705 | — |
| Reactant | N,N-diethyl-6-methyl-2-(4-pyridinyl)-4-pyrimidinamine dihydrochloride | HCID 12764719 | — |
| Solvent | Ethanol | HCID 702 | — |
| Solvent | Water | HCID 962 | — |
| Product | N,N-Diethyl-6-methyl-2-(4-pyridinyl)-4-pyrimidinamine | HCID 12764718 | — |
Reaction Steps
A mixture containing 8.2 g. of 4-chloro-6-methyl-2-(4-pyridinyl)pyrimidine, 8.7 g. of diethylamine hydrochloride, 100 ml. of ethanol, 6 g. of potassium carbonate and 10 ml. of water was refluxed with stirring for eight hours and then concentrated in vacuo to dryness. The residue was swirled in water and the solid collected. The solid was dissolved in boiling isopropyl alcohol, the hot solution treated with decolorizing charcoal and filtered, and the hot filtrate allowed to cool. The filtrate was then saturated with gaseous hydrogen chloride, ether was added to turbidity and the mixture was allowed to stand. The separated solid was collected and dried in vacuo at 80° C. to yield 7.4 g. of N,N-diethyl-6-methyl-2-(4-pyridinyl)-4-pyrimidinamine dihydrochloride, m.p. 205°-208° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | USRE030024 |
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| Source dataset | uspto-grants-1979_06 |
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| ORD ID | ord-179b9f13f14640e5ba8919e1c2e7dc77 |
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| Source note | uspto-grants-1979_06 |
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