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HRID 35252作成日:2026年10月25日

N-Ethyl cyclohexylamine → N-ethyl-N-cyclohexyl-2-(1-methyl-1,2,3,4-tetrazol-5-yl)thio-acetamide

https://huagongshe.com/reaction/35252

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 178482014HCID 178482014—
溶媒TetrahydrofuranHCID 8028—
生成物N-ethyl-N-cyclohexyl-2-(1-methyl-1,2,3,4-tetrazol-5-yl)thio-acetamideHCID 5416738452%

反応手順

2-(1-Methyl-1,2,3,4-tetrazol-5-yl)thio-acetic 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 under ice-cooling, and the mixture is further stirred at room temperature for 2 hours. After distilling off the solvent under reduced pressure, 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 dried over anhydrous sodium sulfate. Chloroform is distilled off and the residue is subjected to column chromatography (Wakogel C-200, eluting solvent, benzene:chloroform=4:1, V/V) to isolate N-ethyl-N-cyclohexyl-2-(1-methyl-1,2,3,4-tetrazol-5-yl)thio-acetamide (yield: 52%) which is recrystallized from ether-petroleum ether, white prisms, m.p. 69°-71° C.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US04766120
出典データセットuspto-grants-1988_08
ORD IDord-b367f873217548f6832be636986c31b9
出典メモuspto-grants-1988_08