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Cesium carbonate → Methyl 5-(6-(3-ethylureido)pyridin-3-yl)-2-oxo-1,2-dihydropyridine-3-carboxylate

HRID 2243025
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Reaktionsgleichung

Reaktionsgleichung von HRID 2243025
[CH2:1]([NH:3][C:4]([NH:6][C:7]1[CH:12]=[CH:11][C:10](B2OC(C)(C)C(C)(C)O2)=[CH:9][N:8]=1)=[O:5])[CH3:2].I[C:23]1[CH:24]=[C:25]([C:30]([O:32][CH3:33])=[O:31])[C:26](=[O:29])[NH:27][CH:28]=1.C(=O)([O-])[O-].[Cs+].[Cs+]>O1CCOCC1.O>[CH2:1]([NH:3][C:4](=[O:5])[NH:6][C:7]1[N:8]=[CH:9][C:10]([C:23]2[CH:24]=[C:25]([C:30]([O:32][CH3:33])=[O:31])[C:26](=[O:29])[NH:27][CH:28]=2)=[CH:11][CH:12]=1)[CH3:2]
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Komponenten

6

Edukt 3

HCID 10796Cesium carbonateHCID 27644652-Hydroxy-5-iodo-nicotinic acid methyl esterHCID 592084346-(3-Ethylureido)pyridine-3-boronic acid pinacol ester2×

Produkt 1

HCID 59208351Methyl 5-(6-(3-ethylureido)pyridin-3-yl)-2-oxo-1,2-dihydropyridine-3-carboxylate

Reagenzien, Katalysatoren, Lösungsmittel 2

HCID 962Water
Lösungsmittel
HCID 312751,4-DioxaneLösungsmittel

Versuchsvorschrift

A solution of N-ethyl-N′-(5-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)pyridin-2-yl)urea (Intermediate 1, 200 mg, 0.69 mmol), methyl 5-iodo-2-oxo-1,2-dihydro-3-pyridinecarboxylate (174 mg, 0.62 mmol), Tetrakispalladium (72.2 mg, 0.06 mmol), and cesium carbonate (224 mg, 0.69 mmol) in dioxane (4 mL) and water (1.000 mL) was heated to 100° C. in microwave for 1 h. The reaction mixture was filtered through Celite and washed with methanol. The resulting solution was concentrated under reduced pressure to give a yellow solid. The solid was triturated with acetone, then collected by filtration and added to hot acetone/water. The solution was cooled to room temperature, and the solid that formed was collected by filtration and placed under high vacuum to remove residual solvent (58 mg). MS (ESP): 317 (M+H+) for C15H16N4O4.

Aufarbeitung

  1. filtrationThe reaction mixture was filtered through Celite
  2. washwashed with methanol
  3. concentrationThe resulting solution was concentrated under reduced pressure
  4. customto give a yellow solid
  5. customThe solid was triturated with acetone
  6. filtrationcollected by filtration
  7. additionadded to hot acetone/water
  8. customthe solid that formed
  9. filtrationwas collected by filtration
  10. customto remove residual solvent (58 mg)

Quellen und Nachweise

ORD-Eintrag
ord-95249974426848dbbfe8f5d14d407fa5
Quelldatensatz
uspto-grants-2010_03
DOI
10.6084/m9.figshare.5104873.v1
Patentnummer
US07674801B2

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