StartseiteMCPWorkbenchSkills
StartseiteWorkbenchBenachrichtigungenMein Bereich
llms.txt · MCP-AnleitungDatenschutz · Nutzungsbedingungen · Supportv1.8.0
  1. Startseite
  2. /Reaktion

1,4-Dioxa-8-azaspiro(4.5)decane → 8-(2-Methoxypyridin-4-yl)-1,4-dioxa-8-azaspiro[4.5]decane

HRID 451533
Notizen
Druckvorschau

Reaktionsgleichung

Reaktionsgleichung von HRID 451533
C1(P(C2CCCCC2)C2C=CC=CC=2C2C=CC=CC=2)CCCCC1.Cl[C:27]1[CH:32]=[CH:31][N:30]=[C:29]([O:33][CH3:34])[CH:28]=1.[O:35]1[C:39]2([CH2:44][CH2:43][NH:42][CH2:41][CH2:40]2)[O:38][CH2:37][CH2:36]1.CC(C)([O-])C.[Na+]>O1CCOCC1.C([O-])(=O)C.[Pd+2].C([O-])(=O)C>[CH3:34][O:33][C:29]1[CH:28]=[C:27]([N:42]2[CH2:43][CH2:44][C:39]3([O:38][CH2:37][CH2:36][O:35]3)[CH2:40][CH2:41]2)[CH:32]=[CH:31][N:30]=1
KomponentenReaktionsbedingungenVersuchsvorschriftAufarbeitungQuellen und NachweiseNotizen zur Reaktion

Komponenten

7

Edukt 4

HCID 674351,4-Dioxa-8-azaspiro(4.5)decaneHCID 27342162-(Dicyclohexylphosphino)biphenylHCID 226385104-Chloro-2-methoxypyridineHCID 23676156Sodium t-butoxide

Produkt 1

HCID 673434058-(2-Methoxypyridin-4-yl)-1,4-dioxa-8-azaspiro[4.5]decane

Reagenzien, Katalysatoren, Lösungsmittel 2

HCID 167845
palladium(II) acetate
Katalysator
HCID 312751,4-DioxaneLösungsmittel2×

Reaktionsbedingungen

Temperatur
130 °C

Versuchsvorschrift

A solution of palladium(II) acetate (62.5 mg, 279 μmol) and 2-(dicyclohexylphosphino) biphenyl (201 mg, 557 μmol) in dioxane (1.5 mL) was stirred under argon at room temperature for 10 minutes, then added to a solution of 4-chloro-2-methoxypyridine (500 mg, 3.48 mmol), 1,4-dioxa-8-azaspiro[4.5]decane (499 mg, 446 μL, 3.48 mmol) and sodium tert-butoxide (502 mg, 5.22 mmol) in dioxane (1.5 mL), degassed and argon bubbled through the reaction during 5 minutes. The reaction mixture was heated in the microwave to 130° C. for 30 minutes. The reaction mixture was filtered through dicalite, water was added to the filtrate and the aqueous phase was extracted three times with ethyl acetate. The combined organic layers were dried over Na2SO4 and the solvent was evaporated. The residue was purified by flash chromatography (silica gel, 70 g, 80% to 100% ethyl acetate in heptane). The title compound was obtained as brown oil (700 mg, 80%).

Aufarbeitung

  1. customdegassed
  2. customargon bubbled through the reaction during 5 minutes
  3. filtrationThe reaction mixture was filtered through dicalite, water
  4. additionwas added to the filtrate
  5. extractionthe aqueous phase was extracted three times with ethyl acetate
  6. dry with materialThe combined organic layers were dried over Na2SO4
  7. customthe solvent was evaporated
  8. customThe residue was purified by flash chromatography (silica gel, 70 g, 80% to 100% ethyl acetate in heptane)

Quellen und Nachweise

ORD-Eintrag
ord-f98662627a0b4c1eba8b41e459c6e905
Quelldatensatz
uspto-grants-2013_07
DOI
10.6084/m9.figshare.5104873.v1
Patentnummer
US08486967B2

Notizen zur Reaktion

Wird geladen…

Auf dieser SeiteKomponentenReaktionsbedingungenVersuchsvorschriftAufarbeitungQuellen und NachweiseNotizen zur Reaktion