HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2043448Generated: October 26, 2026
Aminopyrazine → (S)-N2-[1-(4-fluorophenyl)ethyl]-N6-(pyrazin-2-yl)pyridine-2,6-diamine
https://huagongshe.com/reaction/2043448
Participants
| Role | Name | HCID | Charge |
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| Reactant | Aminopyrazine | HCID 78747 | — |
| Reactant | 2-Dicyclohexylphosphino-2',4',6'-triisoprophylbiphenyl | HCID 11155794 | — |
| Reactant | Sodium t-butoxide | HCID 23676156 | — |
| Reactant | (S)-6-Chloro-N-[1-(4-fluorophenyl)ethyl]pyridine-2-amine | HCID 86620619 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | (S)-N2-[1-(4-fluorophenyl)ethyl]-N6-(pyrazin-2-yl)pyridine-2,6-diamine | HCID 70672048 | 79.1% |
Reaction Steps
207 mg of (S)-6-chloro-N-[1-(4-fluorophenyl)ethyl]pyridine-2-amine, 86 mg of 2-aminopyrazine, 79 mg of 2-dicyclohexylphosphino-2′,4′,6′-triisopropylbiphenyl, 111 mg of sodium t-butoxide and 43 mg of tris(dibenzylideneacetone) (chloroform)dipalladium were added in turn to 4 ml of degassed toluene, and the mixture was stirred at 100° C. for 1 hour under argon atmosphere. The reaction solution was purified by silica gel column chromatography to obtain 202 mg of (S)—N2-[1-(4-fluorophenyl)ethyl]-N6-(pyrazin-2-yl)pyridine-2,6-diamine as pale yellow powder. Furthermore, the obtained compound was subjected to hydrochlorination using a conventional method to obtain 128 mg of the objective compound as pale orange powder.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08586591B2 |
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| Source dataset | uspto-grants-2013_11 |
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| ORD ID | ord-7227f945664b4cb0a41692dd6e212021 |
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| Source note | uspto-grants-2013_11 |
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