Pyridine → HCID 10004788, compound

Participants

Reaction Steps

Using the general method of Example 255, except that pyridine was used in place of acetonitrile, 1-(3-aminobutyl)-2-(3-phenoxypropyl)-1H-imidazo [4,5-c]quinolin-4-amine (2.00 g, 5.1 mmol) was reacted with an excess of methanesulfonic anhydride to provide 1.36 g of N-{4-[4-amino-2-(3-phenoxypropyl)-1H-imidazo[4,5-c]quinolin-1-yl]butyl}methanesulfonamide as a solid, m.p. 156.4–157.1° C. Analysis: Calculated for C24H29N5O3S: % C, 60.48; % H, 6.34; % N, 14.69. Found: % C, 60.75; % H, 6.36; % N, 14.31.

Provenance & Evidence