Reaktion #9607

ord-99bd2886c8094accacefd852ba8f9685

Reaktionsgleichung

CCOC(C)=O
ethyl acetate
CCOCc1nc2c(N)nc3cc(Br)ccc3c2n1CC1CCNCC1.Cl.Cl
7-bromo-2-ethoxymethyl-1-(piperidin-4-ylmethyl)-1H-imidazo[4,5-c]quinolin-4-amine dihydrochloride
CCN(CC)CC
triethylamine
CC(C)C(=O)Cl
isobutyryl chloride
CCOCc1nc2c(N)nc3cc(Br)ccc3c2n1CC1CCN(C(=O)CC(C)C)CC1
7-bromo-2-ethoxymethyl-1-{[1-(2-methylpropylcarbonyl)piperidin-4-yl]methyl}-1H-imidazo[4,5-c]quinolin-4-amine

Lösungsmittel

Reaktionsbedingungen

Detaillierte Bedingungen
See reaction.notes.procedure_details.

Aufarbeitung

  1. 1
    Sonstigethe solid was recrystallized from ethyl acetate
  2. 2
    Sonstigetriturated with hot acetonitrile
  3. 3
    Sonstigeisolated by filtration

Vorschrift

A solution of 7-bromo-2-ethoxymethyl-1-(piperidin-4-ylmethyl)-1H-imidazo[4,5-c]quinolin-4-amine dihydrochloride (4.0 g, 8.1 mmol) and triethylamine (5.67 mL, 40.7 mmol) in chloroform (300 mL) was treated with isobutyryl chloride (0.85 mL, 8.1 mmol) according to the method described in Part A of Examples 583–611. The reaction was complete after one hour. Following trituration with ethyl acetate, the solid was recrystallized from ethyl acetate and then triturated with hot acetonitrile and isolated by filtration to provide 3.63 g of 7-bromo-2-ethoxymethyl-1-{[1-(2-methylpropylcarbonyl)piperidin-4-yl]methyl}-1H-imidazo[4,5-c]quinolin-4-amine as a white solid, mp 199–200° C.

Quelle

DOI: 10.6084/m9.figshare.5104873.v1Patent: US07091214B2uspto-grants-2006_08