Potassium Carbonate → 3-Amino-1-(4-ethylpiperazin-1-yl)isoquinoline

HRID 1814589Notizen

Reaktionsgleichung

Reaktionsgleichung von HRID 1814589
[NH2:1][C:2]1[N:3]=[C:4](Br)[C:5]2[C:10]([CH:11]=1)=[CH:9][CH:8]=[CH:7][CH:6]=2.[CH2:13]([N:15]1[CH2:20][CH2:19][NH:18][CH2:17][CH2:16]1)[CH3:14].C(=O)([O-])[O-].[K+].[K+]>CN(C)C=O>[NH2:1][C:2]1[N:3]=[C:4]([N:18]2[CH2:19][CH2:20][N:15]([CH2:13][CH3:14])[CH2:16][CH2:17]2)[C:5]2[C:10]([CH:11]=1)=[CH:9][CH:8]=[CH:7][CH:6]=2

Komponenten

5

Edukt 3

HCID 11430Potassium CarbonateHCID 791961-EthylpiperazineHCID 2898451-Bromoisoquinolin-3-amine

Produkt 1

HCID 225029343-Amino-1-(4-ethylpiperazin-1-yl)isoquinolineAusbeute 38 %

Reagenzien, Katalysatoren, Lösungsmittel 1

HCID 6228DimethylformamideLösungsmittel

Versuchsvorschrift

3-Amino-1-bromoisoquinoline (10.3 g) and 1-ethylpiperazine (10.5 g) were reacted in the presence of potassium carbonate (13.8 g) in N,N-dimethylformamide (80 ml) at room temperature for 3 days. The reaction solution was concentrated, followed by the addition of purified water (500 ml), and the resulting mixture was stirred under ice-cooling for 1 hr. The resulting ocherous precipitates were collected by filtration, washed with a small amount of ice-water and hexane, and then dried at 50° C. under reduced pressure, to give 3-amino-1-(4-ethylpiperazin-1-yl)isoquinoline (4.5 g).

Aufarbeitung

  1. concentrationThe reaction solution was concentrated
  2. additionfollowed by the addition of purified water (500 ml)
  3. temperaturecooling for 1 hr
  4. customThe resulting ocherous precipitates
  5. filtrationwere collected by filtration
  6. washwashed with a small amount of ice-water and hexane
  7. customdried at 50° C. under reduced pressure

Quellen und Nachweise

ORD-Eintrag
ord-a6a40fbedff246c5a150b5fde3f58f87
Quelldatensatz
uspto-grants-2005_04
Patentnummer
US06875761B2

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