Ammonia → HCID 178508172、化合物

HRID 1187388

反応式

HRID 1187388 の反応式
[C:1]1(S(Cl)(=O)=O)[CH:6]=[CH:5][CH:4]=[CH:3][CH:2]=1.CS(Cl)(=O)=O.[NH3:16].[OH-].[NH4+:18].[C:19](=O)([O-])[O-].[NH4+:23].[NH4+:24].[C:25](=O)(O)[O-].[NH4+:29].P([O-])([O-])([O-])=O.[NH4+].[NH4+].[NH4+].[C:38]1([CH3:48])[CH:43]=[CH:42][C:41](S(Cl)(=O)=O)=[CH:40][CH:39]=1>C(Cl)(Cl)Cl.ClCCl>[NH:16]1[C:2]2[C:3]3[N:24]=[CH:1][CH:6]=[CH:5][C:4]=3[N:23]=[C:39]([NH2:29])[C:38]=2[N:18]=[CH:25]1.[NH:16]1[C:48]2[C:38]3[CH:43]=[CH:42][CH:41]=[CH:40][C:39]=3[N:23]=[C:2]([NH2:24])[C:1]=2[N:18]=[CH:19]1

参加物

12

反応物 8

HCID 222AmmoniaHCID 7369Benzenesulfonyl chlorideHCID 73974-Toluenesulfonyl chlorideHCID 14013Ammonium BicarbonateHCID 14923Ammonium Hydroxide2 回HCID 31297Methanesulfonyl chlorideHCID 159282Ammonium phosphate, tribasicHCID 517111Ammonium Carbonate

生成物 2

HCID 178508172HCID 178508172、化合物HCID 178508191HCID 178508191、化合物

試薬・触媒・溶媒 2

HCID 6212Chloroform溶媒HCID 6344Dichloromethane溶媒

実験手順

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 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.

後処理

  1. customThe reaction
  2. customcan be carried out at ambient temperature
  3. customUnder these reaction conditions
  4. customthe N-phthalimide protecting group is removed

出典と根拠

ORDレコード
ord-7f68d3770fb041af9f58adfa07c9a57f
出典データセット
uspto-grants-2014_03
特許番号
US08673932B2

関連ノート

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