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Ethyl 5-methoxyimidazo[1,2-a]quinoline-2-carboxylate → HCID 13055757, Verbindung

HRID 2166510
Notizen
Druckvorschau

Reaktionsgleichung

Reaktionsgleichung von HRID 2166510
[CH3:1][O:2][C:3]1[C:12]2[C:7](=[CH:8][CH:9]=[CH:10][CH:11]=2)[N:6]2[CH:13]=[C:14]([C:16](OCC)=[O:17])[N:15]=[C:5]2[CH:4]=1.[H-].[Al+3].[Li+].[H-].[H-].[H-]>O1CCCC1>[CH3:1][O:2][C:3]1[C:12]2[C:7](=[CH:8][CH:9]=[CH:10][CH:11]=2)[N:6]2[CH:13]=[C:14]([CH2:16][OH:17])[N:15]=[C:5]2[CH:4]=1
KomponentenVersuchsvorschriftAufarbeitungQuellen und NachweiseNotizen zur Reaktion

Komponenten

4

Edukt 2

HCID 13055756Ethyl 5-methoxyimidazo[1,2-a]quinoline-2-carboxylateHCID 21226445Aluminium lithium hydride

Produkt 1

HCID 13055757HCID 13055757, VerbindungAusbeute 89,2 %

Reagenzien, Katalysatoren, Lösungsmittel 1

HCID 8028TetrahydrofuranLösungsmittel

Versuchsvorschrift

A suspension of 19.71 g (73 mmol) of ethyl 5-methoxyimidazo[1,2-a]quinoline-2-carboxylate in 350 ml of freshly distilled anhydrous tetrahydrofuran was stirred under a nitrogen atmosphere at room temperature and 3.33 g (88 mmol) of lithium aluminum hydride were added thereto in portions over 3 hours. The mixture was stirred for 4 hours and excess hydride was destroyed by dropwise addition of wet tetrahydrofuran followed by water. The mixture was poured into 1.5 liters of water and the mixture was extracted with 500 ml of a chloroform-methanol mixture. The mixture was filtered through a celite pad and the aqueous phase was extracted again with a chloroform-methanol mixture. The combined organic phases were dried over anhydrous magnesium sulfate and evaporated to dryness under reduced pressure. The residue was triturated with ethyl acetate, filtered, washed with ethyl acetate and dried under reduced pressure over P2O5 to obtain 14.87 g (89% yield) of 5-methoxy-imidazo[1,2-a]quinoline-2-methanol as a white crystalline solid melting at 173°-175° C.

Aufarbeitung

  1. stirringThe mixture was stirred for 4 hours
  2. customexcess hydride was destroyed by dropwise addition of wet tetrahydrofuran
  3. additionThe mixture was poured into 1.5 liters of water
  4. extractionthe mixture was extracted with 500 ml of a chloroform-methanol mixture
  5. filtrationThe mixture was filtered through a celite pad
  6. extractionthe aqueous phase was extracted again with a chloroform-methanol mixture
  7. dry with materialThe combined organic phases were dried over anhydrous magnesium sulfate
  8. customevaporated to dryness under reduced pressure
  9. customThe residue was triturated with ethyl acetate
  10. filtrationfiltered
  11. washwashed with ethyl acetate
  12. dry with materialdried under reduced pressure over P2O5

Quellen und Nachweise

ORD-Eintrag
ord-faf7a24c59de4f2788d8691028865a32
Quelldatensatz
uspto-grants-1983_06
DOI
10.6084/m9.figshare.5104873.v1
Patentnummer
US04387098

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