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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1187388생성일: 2026년 10월 26일

Ammonia → HCID 178508172, 화합물

https://huagongshe.com/reaction/1187388

반응식

참여 물질

역할이름HCID투입량
반응물AmmoniaHCID 222—
반응물Benzenesulfonyl chlorideHCID 7369—
반응물4-Toluenesulfonyl chlorideHCID 7397—
반응물Ammonium BicarbonateHCID 14013—
반응물Ammonium HydroxideHCID 14923—
반응물Methanesulfonyl chlorideHCID 31297—
반응물Ammonium phosphate, tribasicHCID 159282—
반응물Ammonium CarbonateHCID 517111—
용매ChloroformHCID 6212—
용매DichloromethaneHCID 6344—
생성물HCID 178508172HCID 178508172—
생성물HCID 178508191HCID 178508191—

반응 단계

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.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08673932B2
출처 데이터셋uspto-grants-2014_03
ORD IDord-7f68d3770fb041af9f58adfa07c9a57f
출처 메모uspto-grants-2014_03