8-Hydroxyquinoline → HCID 89699972, Verbindung

HRID 1055649Notizen

Reaktionsgleichung

Reaktionsgleichung von HRID 1055649
Br[C:2]1[CH:3]=[C:4]([CH:8]=[C:9]([S:11]([F:16])([F:15])([F:14])([F:13])[F:12])[CH:10]=1)[C:5]([OH:7])=[O:6].[CH3:17][C:18]1[NH:19][CH:20]=[CH:21][N:22]=1.OC1C=CC=C2C=1N=CC=C2>CN(C=O)C.C(=O)(O)[O-].C([N+](CC)(CC)CC)C.[Cu]I>[CH3:17][C:18]1[N:19]([C:2]2[CH:3]=[C:4]([CH:8]=[C:9]([S:11]([F:16])([F:15])([F:14])([F:13])[F:12])[CH:10]=2)[C:5]([OH:7])=[O:6])[CH:20]=[CH:21][N:22]=1

Komponenten

7

Edukt 3

HCID 19238-HydroxyquinolineHCID 127492-MethylimidazoleHCID 581374213-Bromo-5-(pentafluorosulfur)benzoic acid

Produkt 1

HCID 89699972HCID 89699972, Verbindung

Reagenzien, Katalysatoren, Lösungsmittel 3

HCID 24350Copper(1+) iodide; Copper(I) iodide; Cuprous iodide; Cuprous iodide (CuI)KatalysatorHCID 11805541Tetraethylammonium bicarbonateKatalysatorHCID 6228DimethylformamideLösungsmittel

Reaktionsbedingungen

Temperatur
160 °C

Versuchsvorschrift

1.0 g (3.06 mmol) of the compound of Example 15A and 276 mg (3.36 mmol) of 2-methylimidazole were dissolved in 20 ml of DMF and 2 ml of water, and the mixture was degassed with argon. 2.06 g (6.42 mmol) of tetraethylammonium bicarbonate were added carefully, followed by 232 mg (1.22 mmol) of copper(I) iodide and 177 mg (1.22 mmol) of 8-hydroxyquinoline. The mixture was heated in a microwave oven (Biotage Initiator, with Dynamic Field Tuning) at 160° C. for 60 min. The reaction was then filtered, and the filtrate was adjusted at pH 1 with concentrated hydrochloric acid and concentrated under reduced pressure. The residue was separated into its components by preparative HPLC (Method 17). Evaporation of the product fractions and drying of the residue under high vacuum gave 238 mg (94% pure, 22% of theory) of the title compound.

Aufarbeitung

  1. custom2 ml of water, and the mixture was degassed with argon
  2. filtrationThe reaction was then filtered
  3. concentrationconcentrated under reduced pressure
  4. customThe residue was separated into its components by preparative HPLC (Method 17)
  5. customEvaporation of the product fractions
  6. customdrying of the residue under high vacuum

Quellen und Nachweise

ORD-Eintrag
ord-96a6f56361a04f6d845369da31940732
Quelldatensatz
uspto-grants-2016_07
Patentnummer
US09394309B2

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