HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 226388Erstellt: 26. Oktober 2026
Diisopropylethylamine → HCID 86603696, Verbindung
https://huagongshe.com/reaction/226388
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Diisopropylethylamine | HCID 81531 | — |
| Edukt | 4-Chloropyrimidine | HCID 642834 | — |
| Edukt | ethyl (2E)-3-{5-[(3R)-3-piperidinylamino]-2-pyrazinyl)acrylate dihydrochloride | HCID 86603669 | — |
| Lösungsmittel | Dimethylformamide | HCID 6228 | — |
| Produkt | HCID 86603696 | HCID 86603696 | 46,3% |
Reaktionsschritte
To a solution of ethyl (2E)-3-{5-[(3R)-3-piperidinylamino]-2-pyrazinyl}acrylate dihydrochloride (300 mg, 0.86 mmol) in DMF (6 mL) were added diisopropylethylamine (366 mg, 2.84 mmol) and 6-chloropyrimidine (128 mg, 1.11 mmol) at ambient temperature and the mixture was stirred at ambient temperature for 18 hrs. The reaction mixture was evaporated in vacuo and the residue was partitioned between water and EtOAc. The organic layer was separated, washed water and brine, dried over magnesium sulfate, and evaporated in vacuo. The residue was purified by silica gel column chromatography (chloroform-MeOH=95-5/hexane-EtOAc=¼) to give ethyl (2E)-3-(5-{[(3R)-1-(2-pyrimidinyl)-3-piperidinyl]amino}-2-pyrazinyl)acrylate (141 mg, 46%) as an amorphous powder.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US07557127B2 |
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| Quelldatensatz | uspto-grants-2009_07 |
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| ORD ID | ord-f2032b5a5059435d879d47024eaa4deb |
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| Quellennotiz | uspto-grants-2009_07 |
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