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HRID 978029作成日:2026年10月25日

N-Ethyl cyclohexylamine → HCID 21295432、化合物

https://huagongshe.com/reaction/978029

反応式

関与物質

役割名称HCID仕込み量
反応物N-Ethyl cyclohexylamineHCID 21609—
反応物Isobutyl chloroformateHCID 62365—
反応物1,8-Diazabicyclo(5.4.0)undec-7-eneHCID 81184—
反応物HCID 178489576HCID 178489576—
溶媒TetrahydrofuranHCID 8028—
生成物HCID 21295432HCID 2129543245%

反応手順

4-[1-(2-Methoxycyclohexyl)-1,2,3,4-tetrazol-5-yl]thio-butyric acid (45 mmole) is dissolved in tetrahydrofuran (50 ml), and thereto is added DBU (50 mmole). To the mixture is added dropwise with stirring isobutyl chloroformate (50 mmole) under ice-cooling, and the mixture is stirred at room temperature for 30 minutes. To the mixture is added dropwise N-ethyl-cyclohexylamine (54 mmole), and the mixture is further stirred at room temperature for 2 hours. The solvent is distilled off under reduced pressure, and the residue is extracted with chloroform. The chloroform layer is washed with 5% aqueous hydrochloric acid, an aqueous saturated sodium hydrogen carbonate solution and an aqueous saturated sodium chloride solution and then dried over anhydrous sodium sulfate. After distilling off chloroform, the resulting residue is subjected to column chromatography (Wakogel C-200, eluting solvent, benzene:chlororform=4:1, V/V) to isolate N-ethyl-N-cyclohexyl-4-[1-(2-methoxycyclohexyl)-1,2,3,4-tetrazol-5-yl]thio-butyramide (yield: 45%).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US04663323
出典データセットuspto-grants-1987_05
ORD IDord-d0c1a78f34f34ebda184f304400986e1
出典メモuspto-grants-1987_05