Zurück
HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1187388Erstellt: 26. Oktober 2026

Ammonia → HCID 178508172, Verbindung

https://huagongshe.com/reaction/1187388

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktAmmoniaHCID 222—
EduktBenzenesulfonyl chlorideHCID 7369—
Edukt4-Toluenesulfonyl chlorideHCID 7397—
EduktAmmonium BicarbonateHCID 14013—
EduktAmmonium HydroxideHCID 14923—
EduktMethanesulfonyl chlorideHCID 31297—
EduktAmmonium phosphate, tribasicHCID 159282—
EduktAmmonium CarbonateHCID 517111—
LösungsmittelChloroformHCID 6212—
LösungsmittelDichloromethaneHCID 6344—
ProduktHCID 178508172HCID 178508172—
ProduktHCID 178508191HCID 178508191—

Reaktionsschritte

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 XXIX is aminated to provide a 1H-imidazo[4,5-c][1,5]naphthyridinamine or 1H-imidazo[4,5-c]quinolin-4-amine of Formula XXX. Step (10) involves the activation of an N-oxide of Formula XXIX 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, orp-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 XXX 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]naphthyridin4-amine or 1H-imidazo[4,5-c]quinolin-4-amine of Formula XXX or a pharmaceutically acceptable salt thereof, which can be isolated from the reaction mixture using conventional methods.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08673932B2
Quelldatensatzuspto-grants-2014_03
ORD IDord-7f68d3770fb041af9f58adfa07c9a57f
Quellennotizuspto-grants-2014_03