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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1992576Generated: October 26, 2026

Ammonia → HCID 178508172, compound

https://huagongshe.com/reaction/1992576

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAmmoniaHCID 222—
ReactantBenzenesulfonyl chlorideHCID 7369—
Reactant4-Toluenesulfonyl chlorideHCID 7397—
ReactantAmmonium BicarbonateHCID 14013—
ReactantAmmonium HydroxideHCID 14923—
ReactantMethanesulfonyl chlorideHCID 31297—
ReactantAmmonium phosphate, tribasicHCID 159282—
ReactantAmmonium CarbonateHCID 517111—
SolventChloroformHCID 6212—
SolventDichloromethaneHCID 6344—
ProductHCID 178508172HCID 178508172—
ProductHCID 178508191HCID 178508191—

Reaction Steps

In step (10) of Reaction Scheme I, a 1H-imidazo[4,5-c][1,5]naphthyridine-5N-oxide or 1H-imidazo[4,5-c]quinoline-5N-oxide of Formula XXIV is aminated to provide a 1H-imidazo[4,5-c][1,5]naphthyridin-4-amine or 1H-imidazo[4,5-c]quinolin-4-amine of Formula XXV. Step (10) involves the activation of an N-oxide of Formula XXIV by conversion to an ester and then reacting the ester with an aminating agent. Suitable activating agents include alkyl- or arylsulfonyl chlorides such as benzenesulfonyl chloride, methanesulfonyl chloride, or p-toluenesulfonyl chloride. Suitable aminating agents include ammonia, in the form of ammonium hydroxide, for example, and ammonium salts such as ammonium carbonate, ammonium bicarbonate, and ammonium phosphate. The reaction is conveniently carried out by adding ammonium hydroxide to a solution of the N-oxide of Formula XXIV in a suitable solvent such as dichloromethane or chloroform and then adding p-toluenesulfonyl chloride. The reaction can be carried out at ambient temperature. Under these reaction conditions, the N-phthalimide protecting group is removed to provide the 1H-imidazo[4,5-c][1,5]naphthyridin-4-amine or 1H-imidazo[4,5-c]quinolin-4-amine of Formula XXV or a pharmaceutically acceptable salt thereof, which can be isolated from the reaction mixture using conventional methods.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07648997B2
Source datasetuspto-grants-2010_01
ORD IDord-01a3e13e10e24917aa6a2f69b610fbe8
Source noteuspto-grants-2010_01