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HRID 1719586作成日:2026年10月27日

N-Ethyl cyclohexylamine → N-ethyl-N-cyclohexyl-4-[1-(4-ethylphenyl)-1,2,3,4-tetrazol-5-yl]thio-butyramide

https://huagongshe.com/reaction/1719586

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 178436515HCID 178436515—
溶媒TetrahydrofuranHCID 8028—
生成物N-ethyl-N-cyclohexyl-4-[1-(4-ethylphenyl)-1,2,3,4-tetrazol-5-yl]thio-butyramideHCID 5406090843%

反応手順

4-[1-(4-Ethylphenyl)-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 mmol) 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 resulting 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. Chloroform is distilled off and the resulting residue is subjected to column chromatography (Wakogel C-200, eluting solvent, benzene:chloroform=4:1, V/V) to isolate N-ethyl-N-cyclohexyl-4-[1-(4-ethylphenyl)-1,2,3,4-tetrazol-5-yl]thio-butyramide (yield: 43%), colorless liquid, nD19 =1.5533.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US04540703
出典データセットuspto-grants-1985_09
ORD IDord-b8d94aaf9aca4320aaab1d0dc31d6c9d
出典メモuspto-grants-1985_09