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

m-Chloroperbenzoic acid → 1-(benzyloxy)-2-propyl-1H-imidazo[4,5-c]quinolin-4-amine

HRID 2105461
Notizen
Druckvorschau

Reaktionsgleichung

Reaktionsgleichung von HRID 2105461
[CH2:1]([O:8][N:9]1[C:21]2[C:20]3[CH:19]=[CH:18][CH:17]=[CH:16][C:15]=3[N:14]=[CH:13][C:12]=2[N:11]=[C:10]1[CH2:22][CH2:23][CH3:24])[C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=1.ClC1C=C(C=CC=1)C(OO)=O.ClC(Cl)(Cl)C([N:40]=C=O)=O>ClCCl>[CH2:1]([O:8][N:9]1[C:21]2[C:20]3[CH:19]=[CH:18][CH:17]=[CH:16][C:15]=3[N:14]=[C:13]([NH2:40])[C:12]=2[N:11]=[C:10]1[CH2:22][CH2:23][CH3:24])[C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=1
KomponentenReaktionsbedingungenVersuchsvorschriftAufarbeitungQuellen und NachweiseNotizen zur Reaktion

Komponenten

5

Edukt 3

HCID 70297m-Chloroperbenzoic acidHCID 76400Trichloroacetyl isocyanateHCID 675064061-benzyloxy-2-propyl-1H-imidazo[4,5-c]quinoline

Produkt 1

HCID 575388311-(benzyloxy)-2-propyl-1H-imidazo[4,5-c]quinolin-4-amineAusbeute 40,7 %

Reagenzien, Katalysatoren, Lösungsmittel 1

HCID 6344DichloromethaneLösungsmittel

Reaktionsbedingungen

Temperatur
0 °C

Versuchsvorschrift

A solution of 1-(benzyloxy)-2-propyl-1H-imidazo[4,5-c]quinoline (2.6 g, 8.2 mmol) in dichloromethane (100 mL) was cooled to approximately 0° C., and 3-chloroperoxybenzoic acid (3.6 g of approximately 77% pure material, 16 mmol) was added over a period of several minutes. The reaction was stirred for ten minutes at 0° C., stirred for 90 minutes at room temperature, washed with saturated aqueous sodium bicarbonate (2×35 mL, containing 1 mL of 25% w/w aqueous sodium hydroxide), dried over potassium carbonate, and filtered. The resulting solution was cooled to 0° C., and trichloroacetyl isocyanate (1.22 mL, 10.3 mmol) was added with stirring. The reaction was stirred for 15 minutes at 0° C., stirred for 75 minutes at room temperature, and concentrated under reduced pressure. The residue was dissolved in methanol (60 mL), and sodium methoxide (6.3 mL of a 25% w/w solution in methanol, 29 mmol) was added with stirring. The mixture was stirred at room temperature overnight. A precipitate formed, and the reaction mixture was cooled to approximately 0° C. The precipitate was collected by filtration, recrystallized from methanol/water, and dried overnight in a vacuum oven at 70° C. to provide 1.11 g of 1-(benzyloxy)-2-propyl-1H-imidazo[4,5-c]quinolin-4-amine as white crystals, mp 164-166° C.

Aufarbeitung

  1. stirringstirred for 90 minutes at room temperature
  2. washwashed with saturated aqueous sodium bicarbonate (2×35 mL, containing 1 mL of 25% w/w aqueous sodium hydroxide)
  3. dry with materialdried over potassium carbonate
  4. filtrationfiltered
  5. temperatureThe resulting solution was cooled to 0° C.
  6. stirringwith stirring
  7. stirringThe reaction was stirred for 15 minutes at 0° C.
  8. stirringstirred for 75 minutes at room temperature
  9. concentrationconcentrated under reduced pressure
  10. dissolutionThe residue was dissolved in methanol (60 mL)
  11. additionsodium methoxide (6.3 mL of a 25% w/w solution in methanol, 29 mmol) was added
  12. stirringwith stirring
  13. stirringThe mixture was stirred at room temperature overnight
  14. customA precipitate formed
  15. temperaturethe reaction mixture was cooled to approximately 0° C
  16. filtrationThe precipitate was collected by filtration
  17. customrecrystallized from methanol/water
  18. customdried overnight in a vacuum oven at 70° C.

Quellen und Nachweise

ORD-Eintrag
ord-8e73b2786fa3481488585593c9916879
Quelldatensatz
uspto-grants-2009_08
DOI
10.6084/m9.figshare.5104873.v1
Patentnummer
US07579359B2

Notizen zur Reaktion

Wird geladen…

Auf dieser SeiteKomponentenReaktionsbedingungenVersuchsvorschriftAufarbeitungQuellen und NachweiseNotizen zur Reaktion