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1,4-Dioxane--water (1/1) → HCID 178519752, Verbindung

HRID 2374161
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Druckvorschau

Reaktionsgleichung

Reaktionsgleichung von HRID 2374161
[CH:1]1([C:4]2[NH:13][C:7]3=[N:8][CH:9]=[CH:10][C:11]([CH3:12])=[C:6]3[N:5]=2)[CH2:3][CH2:2]1.[O:14]1CCOCC1.O>>[CH:1]1([C:4]2[NH:13][C:7]3=[N:8][CH:9]=[CH:10][C:11]([CH:12]=[O:14])=[C:6]3[N:5]=2)[CH2:3][CH2:2]1
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Komponenten

3

Edukt 2

HCID 218864351,4-Dioxane--water (1/1)HCID 178428356HCID 178428356, Verbindung

Produkt 1

HCID 178519752HCID 178519752, Verbindung

Versuchsvorschrift

2-Cyclopropyl-7-methyl-3H-imidazo[4,5-b]pyridine (100 mg, 0.58 mmol; from EP0420237 A1) was treated with SeO2 (160 mg, 1.44 mmol) in 6 ml of dioxane:water (4:1) and subjected to microwave irradiation (300 W, normal absorbance) at 180° C. for three 20 min interyals. The mixture was subsequently treated with satd. aq. NaHCO3 (25 ml) and water (25 ml) and the solids were removed by filtration through Celite, rinsing with DCM. The filtrate was extracted with DCM (4×50 mL) and the combined organic extracts were dried (Na2SO4), filtered, and concentrated to dryness to yield the crude title compound. MS (ESI+) for m/z 188 (M+H)+.

Aufarbeitung

  1. customsubjected to microwave irradiation (300 W, normal absorbance) at 180° C. for three 20 min interyals
  2. addition
The mixture was subsequently treated with satd
  • customaq. NaHCO3 (25 ml) and water (25 ml) and the solids were removed by filtration through Celite
  • washrinsing with DCM
  • extractionThe filtrate was extracted with DCM (4×50 mL)
  • dry with materialthe combined organic extracts were dried (Na2SO4)
  • filtrationfiltered
  • concentrationconcentrated to dryness
  • Quellen und Nachweise

    ORD-Eintrag
    ord-c7164df1ca0d4e3cb01416dbd3f1de79
    Quelldatensatz
    uspto-grants-2008_12
    DOI
    10.6084/m9.figshare.5104873.v1
    Patentnummer
    US07462600B2

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