1278739 Anilino-salicylic acid derivatives MERCK & CO Inc 18 June 1970 [25 June 1969 20 April 1970] 29541/70 Heading C2C Novel compounds of Formula I in which R is hydrogen and X is fluorine, alkylthio, alkylsulfinyl, alkylsulfonyl, dialkylamino or alkylamino, or R is alkyl and X is hydrogen, alkyl, hydroxy, alkoxy, acyloxy, halogen, haloalkyl, nitro, amino, alkylamino, dialkylamino, acylamino, mercapto, alkylthio, alkylsulfinyl, alkylsulfonyl, sulfamoyl, aminoalkyl, alkylaminoalkyl, hydroxyalkyl, alkoxyalkyl, mercaptoalkyl alkylmercaptoalkyl, cyano, carboxy, carboalkoxy, carbamoyl, aryl, aralkyl, aryloxy or aralkoxy; R 1 is hydroxy, amino, alkoxy, alkylamino, dialkylamino, dialkylaminoalkylamino, dialkylaminoalkoxy, hydroxyalkoxy, polyhydroxyalkoxy, alkoxyalkoxy, phenylalkoxy, phenoxy, alkoxyphenoxy, dialkylaminophenoxy, halophenoxy, alkanoylaminophenoxy, anilino, alkanoylaminoalkoxy, hydrazino, hydroxylamino, N- morpholino, hydroxyalkylamino or a radical derived from a naturally occurring amino acid and attached at the N atom; R 2 is hydrogen, acyl, alkyl or alkoxy carbonyl; and R 3 is hydrogen, halogen, haloalkyl, alkyl, cycloalkyl or alkoxy, the anilino portion of the substituted anilino carboxylic acid is connected to the 4 or 5 position of the salicylic acid residue the said alkyl and alkoxy radicals and residues contain not more than five carbon atoms and the said alkanoyl radicals and residues contain not more than six carbon atoms; or a non-toxic pharmaceutically acceptable salt thereof, are prepared by carboxylating a compound of Formula IIa for example, with an alkali metal carbonate and carbon dioxide, and optionally introducing R 1 and R 2 where there are other than OH or H and/or converting one X group into another and/or salt formation. Amino-phenols of Formula VI are prepared by demethylation of the corresponding methyl ether obtained by introduction of R into a compound of formula IV prepared by reaction of a substituted aniline and a halophenol methyl ether. Pharmaceutical compositions in conventional forms for oral, parenteral, rectal or topical administration having anti - inflammatory activity comprise an above novel compound and a carrier or diluent therefor.
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机译:1278739苯胺-水杨酸衍生物MERCK&CO Inc 1970年6月18日[1969年6月25日1970年4月20日]标题C2C其中R为氢且X为氟,烷硫基,烷基亚磺酰基,烷基磺酰基,二烷基氨基或烷基氨基的式I新型化合物,或R为烷基,X为氢,烷基,羟基,烷氧基,酰氧基,卤素,卤代烷基,硝基,氨基,烷基氨基,二烷基氨基,酰基氨基,巯基,烷硫基,烷基亚磺酰基,烷基磺酰基,氨磺酰基,氨基烷基,烷基氨基烷基,羟烷基,烷氧基烷基,巯基烷基烷基巯基烷基,氰基,羧基,碳烷氧基,氨基甲酰基,芳基,芳烷基,芳氧基或芳烷氧基; R 1是羟基,氨基,烷氧基,烷基氨基,二烷基氨基,二烷基氨基烷基氨基,二烷基氨基烷氧基,羟基烷氧基,多羟基烷氧基,烷氧基烷氧基,苯基烷氧基,苯氧基,烷氧基苯氧基,二烷基氨基苯氧基,卤代苯氧基,链烷酰基氨基苯氧基,苯胺基,烷酰基氨基烷氧基,氨基-氨基羟基或氨基源自天然氨基酸并连接在N原子上的基团; R 2是氢,酰基,烷基或烷氧基羰基;并且R 3是氢,卤素,卤代烷基,烷基,环烷基或烷氧基,取代的苯胺羧酸的苯胺基部分连接至水杨酸残基的4或5位,所述烷基和烷氧基和残基不超过五个碳原子,并且所述烷酰基基团和残基包含不超过六个碳原子;或其无毒的药学上可接受的盐,是通过例如将式IIa的化合物与碱金属碳酸盐和二氧化碳进行羧化,并在不存在OH或H和/或将一个X基团转化为另一个和/或形成盐。式Ⅵ的氨基酚是通过将相应的甲醚脱甲基而制得的,该甲醚是通过将R引入到由取代的苯胺和卤代苯酚甲醚反应制得的式Ⅳ化合物中而得到的。具有抗炎活性的用于口服,肠胃外,直肠或局部给药的常规形式的药物组合物包含上述新型化合物及其载体或稀释剂。
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