首页> 外国专利> 2,4-DISUBSTITUTED-5-AMINOCARBONYL-1,3-THIAZOLE DERIVATIVES FOR THERAPEUTIC AGENT OF ANTIINFLAMMATORY DISEASE, METHOD THEREOF FOR PREPARATION, THERAPEUTIC AGENT FOR ANTIINFLAMMATORY DISEASE INDUCED BY SPC ACTIVITY CONTAINING THE SAME

2,4-DISUBSTITUTED-5-AMINOCARBONYL-1,3-THIAZOLE DERIVATIVES FOR THERAPEUTIC AGENT OF ANTIINFLAMMATORY DISEASE, METHOD THEREOF FOR PREPARATION, THERAPEUTIC AGENT FOR ANTIINFLAMMATORY DISEASE INDUCED BY SPC ACTIVITY CONTAINING THE SAME

机译:2,4-二取代的5-氨基羰基-1,3-噻唑衍生物用于抗炎性疾病的治疗剂,其制备方法,由包含相同成分的SPC活性诱导的抗炎性疾病的治疗剂

摘要

PURPOSE: A 2,4-double substitution-5-aminocarbonyl-1,3-thiazole derivative is provided to suppress sphingosylphosphorylcholine(SPC) receptor and to treat diseases caused by SPC receptor. CONSTITUTION: A method for preparing 2,4-double substitution-5-aminocarbonyl-1,3-thiazole derivative of chemical formula 1 comprises: a step of reacting 2-chloroacetoamide derivative with thio aminocarbonate to obtain a compound of chemical formula 3; a step of polymerizing chloridation carboxylic acid with 4-amino group of the compound of chemical formula 3 to obtain a compound of chemical formula 4; a step of oxidizing sulfanyl linker resin part of the compound of chemical formula 4 to synthesize the compound of chemical formula 5; and a step of performing deintercalation and addition of the compound of chemical formula 5. A therapeutic agent for inflammatory disease caused by SPC receptor activation contains the 2,4-double substitution-5-aminocarbonyl-1,3-thiazole derivative of chemical formula 1 or pharmaceutically acceptable salt as an active ingredient.
机译:目的:提供2,4-双取代-5-氨基羰基-1,3-噻唑衍生物以抑制鞘氨醇磷酸胆碱(SPC)受体并治疗由SPC受体引起的疾病。组成:一种化学式1的2,4-双取代-5-氨基羰基-1,3-噻唑衍生物的制备方法,包括:使2-氯乙酰胺衍生物与硫代氨基碳酸酯反应得到化学式3的化合物的步骤;将氯化羧酸与化学式3的化合物的4-氨基聚合得到化学式4的化合物的步骤;氧化化学式4的化合物的硫烷基连接基树脂部分以合成化学式5的化合物的步骤;本发明涉及由SPC受体活化引起的炎性疾病的治疗剂,其包含化学式1的2,4-双取代-5-氨基羰基-1,3-噻唑衍生物。或药学上可接受的盐作为有效成分。

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