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  • Title: [Antimalarial active 10 H-indolo(3,2-b)quinolin-11-yl-amine. 2. Chloroquine analogs].
    Author: Görlitzer K, Stockmann R, Walter RD.
    Journal: Pharmazie; 1995 Feb; 50(2):105-11. PubMed ID: 7700962.
    Abstract:
    The quinolones 1b and 1c react with tosylisocyanate to yield the tosylamino quinolines 2b and 2c, while 1a under the same conditions gives the carbamate 5. Decarboxylation of 5 affords 2a. The mono and bis alkylated products 3 and 6 are received from 2b. The N-tosyl derivatives 2b and 3 rearrange to form the C-tosyl compounds 7 by heating with polyphosphoric acid (PPA) while 2c is hydrolized to 8c. 8 are isolated either from 2 using sulfuric acid 90% or from the 11-chloro-quinolines 9 melting in a mixture of ammonium chloride and acetate. The chloroquine analogues 4 are obtained from the 9-hydrochlorides with the dihydrochloride of the novaldiamine base. The quaternary salt 10 prepared by methylation of 9b reacts with the base in ethanol to yield 11. 4c inhibits the multi-resistant Plasmodium falciparum strain K-1 stronger than chloroquine.
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