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HRID 244902作成日:2026年10月26日

Pyridine → HCID 178499328、化合物

https://huagongshe.com/reaction/244902

反応式

関与物質

役割名称HCID仕込み量
反応物PyridineHCID 1049—
反応物5-(3,3-Dimethyl-but-1-ynyl)-3-(4-[1,2,3]triazol-1-yl-cyclohexylamino)-thiophene-2-carboxylic acid methyl esterHCID 24988980—
反応物HCID 178461265HCID 178461265—
溶媒TolueneHCID 1140—
溶媒Ethyl AcetateHCID 8857—
生成物HCID 178499328HCID 178499328—

反応条件

温度105 °C

反応手順

To a solution of 5-(3,3-dimethyl-but-1-ynyl)-3-(4-[1,2,3]triazol-1-yl-cyclohexylamino)-thiophene-2-carboxylic acid methyl ester (0.20 g, 0.50 mmol) in toluene (1 ml) is added a solution of trans-4-methylcyclohexyl carboxylic acid chloride 1 M (1.0 ml, 1.0 mmol) and pyridine (0.046 ml, 0.58 mmol). The mixture is stirred overnight at 105° C. and diluted with ethyl acetate. The organic layer is washed with NaHCO3 sat (2×) and brine. The organic layer is dried with sodium sulfate, filtered and concentrated under reduce pressure. The residue is purified by silica gel column chromatography (20% ethyl acetate/hexane to 100% ethyl acetate followed by 10% MeOH/ethyl acetate) to give 5-(3,3-dimethyl-but-1-ynyl)-3-[(trans-4-methyl-cyclohexanecarbonyl)-(4-[1,2,3]triazol-1-yl-cyclohexyl)-amino]-thiophene-2-carboxylic acid methyl ester.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08658674B2
出典データセットuspto-grants-2014_02
ORD IDord-fccec03bc8514ee9805280083166835b
出典メモuspto-grants-2014_02