Reaktion #1905372

ord-b444c7d718424bffa01c333bee990425

Reaktionsgleichung

CC(C)N=C=O
Isopropyl isocyanate
CCCCc1nc2c(N)nc3cc(-c4cccnc4)ccc3c2n1CCN
1-(2-aminoethyl)-2-butyl-7-(pyridin-3-yl)-1H-imidazo[4,5-c]quinolin-4-amine
CCCCc1nc2c(N)nc3cc(-c4cccnc4)ccc3c2n1CCNC(=O)NC(C)C
N-{2-[4-amino-2-butyl-7-(pyridin-3-yl)-1H-imidazo[4,5-c]quinolin-1-yl]ethyl}-N′-(1-methylethyl)urea
Ausbeute 47.8%

Lösungsmittel

Reaktionsbedingungen

Detaillierte Bedingungen
See reaction.notes.procedure_details.

Aufarbeitung

  1. 1
    SonstigeA precipitate formed within 15 minutes
  2. 2
    Sonstigewas isolated by filtration
  3. 3
    Sonstigewas dried overnight in an oven

Vorschrift

Isopropyl isocyanate (0.29 mL, 3.1 mmol) was added slowly to a suspension of 1-(2-aminoethyl)-2-butyl-7-(pyridin-3-yl)-1H-imidazo[4,5-c]quinolin-4-amine (1.13 g, 3.1 mmol) in chloroform (113 mL). A precipitate formed within 15 minutes, was isolated by filtration, and was dried overnight in an oven to provide 0.66 g of N-{2-[4-amino-2-butyl-7-(pyridin-3-yl)-1H-imidazo[4,5-c]quinolin-1-yl]ethyl}-N′-(1-methylethyl)urea as a white solid, mp 240-241° C.

Quelle

DOI: 10.6084/m9.figshare.5104873.v1Patent: US07598382B2uspto-grants-2009_10