Water → 2-[(2-Bromo-3-quinolinyl)methyl]-7-hydroxy-6,7-dihydro-1h-cyclopenta[c]pyridine-1,5(2h)-dione

HRID 47360

Reaktionsgleichung

Reaktionsgleichung von HRID 47360
[H-].[Na+].[Li+].[Br-].[Br:5][C:6]1[C:15]([CH2:16]Br)=[CH:14][C:13]2[C:8](=[CH:9][CH:10]=[CH:11][CH:12]=2)[N:7]=1.[OH2:18].CO[CH2:21][CH2:22][O:23]C.[CH3:25][N:26]([CH:28]=[O:29])C>>[Br:5][C:6]1[C:15]([CH2:16][N:26]2[CH:25]=[CH:13][C:8]3[C:9](=[O:18])[CH2:10][CH:22]([OH:23])[C:21]=3[C:28]2=[O:29])=[CH:14][C:13]2[C:8](=[CH:9][CH:10]=[CH:11][CH:12]=2)[N:7]=1

Komponenten

6

Edukt 5

HCID 962WaterHCID 24758Sodium hydrideHCID 82050Lithium BromideHCID 6133242-Bromo-3-(bromomethyl)quinolineHCID 18463208dimethoxyethane N,N-dimethylformamide

Produkt 1

HCID 111766042-[(2-Bromo-3-quinolinyl)methyl]-7-hydroxy-6,7-dihydro-1h-cyclopenta[c]pyridine-1,5(2h)-dione

Reaktionsbedingungen

Temperatur
80 °C

Versuchsvorschrift

0.6 mmol (18 mg) of NaH as an 80% dispersion in mineral oil is added in small fractions to a solution, stirred at 0° C. of 0.6 mmol (100 mg) of the compound described in Preparation A in 20 ml of a DME/DMF mixture (16/4 (v/v)). The mixture is stirred at 0° C. for 10 minutes before the addition, at that temperature, of 2.4 mmol (210 mg) of LiBr. After returning to room temperature, the reaction mixture is stirred for ¼ hour before the addition of 0.66 mmol (200 mg) of 2-bromo-3-bromomethylquinoline. The reaction mixture is then heated at 80° C. for 20 hours and, after returning to room temperature, subsequently poured into a large excess of water. The precipitate that forms is filtered off and washed with ether to yield the expected product.

Aufarbeitung

  1. customAfter returning to room temperature
  2. customafter returning to room temperature
  3. filtrationThe precipitate that forms is filtered off
  4. washwashed with ether

Quellen und Nachweise

ORD-Eintrag
ord-b0f66bd89f8b41cab98c5a373fd8dd35
Quelldatensatz
uspto-grants-2004_03
Patentnummer
US06699876B2

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