HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 372637Generated: October 26, 2026
Ethylamine → 4,6-Dichloro-2-ethylamino-5-pyrimidinecarbonitrile
https://huagongshe.com/reaction/372637
Participants
| Role | Name | HCID | Charge |
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| Reactant | Ethylamine | HCID 6341 | — |
| Reactant | 2,4,6-Trichloro-5-cyanopyrimidine | HCID 250945 | — |
| Solvent | Acetone | HCID 180 | — |
| Product | 4,6-Dichloro-2-ethylamino-5-pyrimidinecarbonitrile | HCID 20510256 | — |
Reaction Steps
A stirred solution of 12.9 grams of 2,4,6-trichloro-5-pyrimidinecarbonitrile in 150 ml of acetone was cooled to -10°, and 7.7 grams of an aqueous 70% ethylamine solution was added dropwise during 2 hours. The temperature of the reaction mixture was maintained at -10° throughout the addition. Following complete addition, the reaction mixture was allowed to warm to room temperature, where it stood for 16 hours. Then most of the acetone was removed by evaporation under reduced pressure. The residue was extracted with a mixture of water and diethyl ether. The ether layer was separated and dried over magnesium sulfate. The dried ether layer was filtered, and the ether was removed under reduced pressure. The residue was recrystallized from a mixture of methylcyclohexane and benzene, then from carbon tetrachloride, to give 4.2 grams of 4,6-dichloro-2-ethylamino-5-pyrimidinecarbonitrile; mp, 145-150°.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04092150 |
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| Source dataset | uspto-grants-1978_05 |
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| ORD ID | ord-82b021f87c5c4064bcb8e4d668f423d2 |
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| Source note | uspto-grants-1978_05 |
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