HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 80918Erstellt: 24. Oktober 2026
(3-Acetamidophenyl)boronic acid → N-{3-[6-(4-Isopropylpiperazin-1-yl)-4-methylpyridin-3-yl]phenyl}acetamide
https://huagongshe.com/de/reaction/80918
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
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| Edukt | (3-Acetamidophenyl)boronic acid | HCID 157274 | — |
| Edukt | 1-(5-Bromo-4-methyl-pyridin-2-yl)-4-isopropyl-piperazine | HCID 58006617 | — |
| Katalysator | HCID 178418397 | HCID 178418397 | — |
| Lösungsmittel | Water | HCID 962 | — |
| Lösungsmittel | 1,4-Dioxane | HCID 31275 | — |
| Produkt | N-{3-[6-(4-Isopropylpiperazin-1-yl)-4-methylpyridin-3-yl]phenyl}acetamide | HCID 15951458 | — |
Reaktionsschritte
To a solution of 1-(5-bromo-4-methyl-pyridin-2-yl)-4-isopropyl-piperazine (0.59 g, 2 mmol) in 1,4-dioxane (12 mL) and water (3 mL) was added 3-acetylamino-phenylboronic acid (430 mg, 2.4 mmol), Pd(PPh3)4 (231 mg, 0.2 mmol) and TEA (404 mg, 4 mmol). The resulting mixture was degassed and heated at 100° C. for 4 h under a nitrogen atmosphere. The mixture was diluted with EtOAc and water. The organic layer was separated and the aqueous phase was extracted with EtOAc. The combined organic layers were washed with brine, dried (Na2SO4), concentrated and purified by chromatography on silica gel eluting with CH2Cl2/MeOH (100:1). This afforded 138 mg (15%) of the title compound.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US08846677B2 |
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| Quelldatensatz | uspto-grants-2014_09 |
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| ORD ID | ord-f75d2e6e2a274443a10f6b15a0c021c6 |
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| Quellennotiz | uspto-grants-2014_09 |
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