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HRID 1992576作成日:2026年10月26日

Ammonia → HCID 178508172、化合物

https://huagongshe.com/reaction/1992576

反応式

関与物質

役割名称HCID仕込み量
反応物AmmoniaHCID 222—
反応物Benzenesulfonyl chlorideHCID 7369—
反応物4-Toluenesulfonyl chlorideHCID 7397—
反応物Ammonium BicarbonateHCID 14013—
反応物Ammonium HydroxideHCID 14923—
反応物Methanesulfonyl chlorideHCID 31297—
反応物Ammonium phosphate, tribasicHCID 159282—
反応物Ammonium CarbonateHCID 517111—
溶媒ChloroformHCID 6212—
溶媒DichloromethaneHCID 6344—
生成物HCID 178508172HCID 178508172—
生成物HCID 178508191HCID 178508191—

反応手順

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.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07648997B2
出典データセットuspto-grants-2010_01
ORD IDord-01a3e13e10e24917aa6a2f69b610fbe8
出典メモuspto-grants-2010_01