HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1775357Generated: November 1, 2026
Piperazine → 5-Chloro-4,6-dimethyl-2-(piperazin-1-yl)pyridine-3-carbonitrile
https://huagongshe.com/reaction/1775357
Participants
| Role | Name | HCID | Charge |
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| Reactant | Piperazine | HCID 4837 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 2,5-Dichloro-4,6-dimethylpyridine-3-carbonitrile | HCID 334852 | — |
| Product | 5-Chloro-4,6-dimethyl-2-(piperazin-1-yl)pyridine-3-carbonitrile | HCID 89825590 | 93% |
Reaction Steps
A mixture of 2,5-dichloro-4,6-dimethylnicotinonitrile (200 mg, 0.995 mmol), K2CO3 (275 mg, 1.990 mmol) and piperazine (5141 mg, 59.7 mmol) was heated under microwave heating at 120° C. for 15 minutes. After cooling to room temperature the mixture was partitioned between 1N HCl and DCM. The layers were separated and the aqueous layer was extracted once with DCM, basified with NaOH (4N) and extracted with DCM (4×). The combined organic layers were dried (sodium sulfate) and concentrated under reduced pressure to give 231 mg of a solid (0.922 mmol, yield 93%) MS (multi-mode) m/z=251.2 [M+1]+.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09260441B2 |
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| Source dataset | uspto-grants-2016_02 |
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| ORD ID | ord-34fe9bdd99214a1f8ea6dd5d98de2860 |
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| Source note | uspto-grants-2016_02 |
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