Wright J B, Hall C M, Johnson H G
J Med Chem. 1978 Sep;21(9):930-5. doi: 10.1021/jm00207a016.
A series of dialkyl N,N'-(m-phenylene)dioxamates was synthesized by treatment of the requisite m-phenylenediamines with an alkyloxalyl chloride in the presence of triethylamine. Hydrolysis with sodium hydroxide solution gave the corresponding N,N'-(m-phenylene)dioxamic acids. Several N,N'-(p-phenylene)dioxamic acids were synthesized also in the same manner starting with the requisite p-phenylenediamines. These compounds were tested in the rat passive cutaneous anaphylaxis (PCA) assay. When tested iv, activity was found in the N,N'-(m-phenylene) dioxamic acids up to 2500 times that shown by disodium cromoglycate [50% inhibition at 0.001 mg/kg for N,N'-(2-chloro-5-cyano-m-phenylene)dioxamic acid (compound 61)]. Oral activity was seen in this series of compounds with duration of activity up to 120 min. Oral activity was detected in diethyl N,N'-(2-chloro-5-cyano-m-phenylene)dioxamate (compound 38) at levels of drug as low as 0.1 mg/kg.
通过在三乙胺存在下,用烷基草酰氯处理所需的间苯二胺,合成了一系列N,N'-(间亚苯基)草酰胺酸二烷基酯。用氢氧化钠溶液水解得到相应的N,N'-(间亚苯基)草酰胺酸。也以同样的方式从所需的对苯二胺开始合成了几种N,N'-(对亚苯基)草酰胺酸。这些化合物在大鼠被动皮肤过敏反应(PCA)试验中进行了测试。静脉注射测试时,发现N,N'-(间亚苯基)草酰胺酸的活性高达色甘酸二钠的2500倍[对于N,N'-(2-氯-5-氰基间亚苯基)草酰胺酸(化合物61),在0.001mg/kg时50%抑制]。在这一系列化合物中观察到口服活性,活性持续时间长达120分钟。在二乙基N,N'-(2-氯-5-氰基间亚苯基)草酰胺酸酯(化合物38)中检测到口服活性,药物水平低至0.1mg/kg。