Sodium Hydroxide → 2-Amino-3-cyano-4-chloro-6-(morpholin-4-yl)quinoline

HRID 1985664Notizen

Reaktionsgleichung

Reaktionsgleichung von HRID 1985664
[NH2:1][C:2]1[C:11]([C:12]#[N:13])=[C:10](O)[C:9]2[C:4](=[CH:5][CH:6]=[C:7]([N:15]3[CH2:20][CH2:19][O:18][CH2:17][CH2:16]3)[CH:8]=2)[N:3]=1.P(Cl)(Cl)([Cl:23])=O.[OH-].[Na+]>>[NH2:1][C:2]1[C:11]([C:12]#[N:13])=[C:10]([Cl:23])[C:9]2[C:4](=[CH:5][CH:6]=[C:7]([N:15]3[CH2:20][CH2:19][O:18][CH2:17][CH2:16]3)[CH:8]=2)[N:3]=1

Komponenten

4

Edukt 3

HCID 14798Sodium HydroxideHCID 24813Phosphorus oxychlorideHCID 178510459HCID 178510459, Verbindung

Produkt 1

HCID 668504532-Amino-3-cyano-4-chloro-6-(morpholin-4-yl)quinoline

Reaktionsbedingungen

Temperatur
120 °C

Versuchsvorschrift

The mixture of 1.7 g of 2-amino-3-cyano-4-hydroxy-6-(morpholin-4-yl)quinoline and 3.4 mL of phosphoryl chloride is stirred at 120° C. for 4 hours. The cooled reaction mixture is poured onto 30 g of ice, the pH of the mixture is adjusted to 8 with 10% NaOH solution, and the precipitated material is filtered off. After drying 1.5 g of the title compound is obtained, m.p.: 206° C.

Aufarbeitung

  1. customThe cooled reaction mixture
  2. filtrationthe precipitated material is filtered off
  3. dry with materialAfter drying 1.5 g of the title compound
  4. customis obtained

Quellen und Nachweise

ORD-Eintrag
ord-ed71a35a850040c7a1b9499941c9c29c
Quelldatensatz
uspto-grants-2009_06
Patentnummer
US07547696B2

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